Process for the preparation of phosphorus-containing compounds

专利摘要:
The invention relates to a process for the preparation of compounds of the formula (I) in which the radical R 1 is selected from -NH 2, -NH 2 -zAz and monovalent alkyl and aryl radicals which each independently of one another are selected from the phosphoryl radicals DOPO, DPhPO and DPhOPO. indices x, y, and z are each independently 0 or 1, where at least one of the indices i = 0, by melamine in a first stage or, if R 1 is an alkyl or aryl radical, the corresponding alkyl or arylguanamine is reacted with one or more of the corresponding phosphinyl chlorides DOP-CI, DPhP-CI and DPhOP-CI to attach one or more phosphinyl residues to the amino group (s) of the melamine or guanamine, and in a second stage the phosphinyl residue (e) is oxidized to the corresponding phosphoryl radical (s) by reaction with an oxidizing agent.
公开号:AT513327A1
申请号:T944/2012
申请日:2012-08-29
公开日:2014-03-15
发明作者:Thomas Zich；Fritz Johann Freidl；Bernadette Mehofer；Manfred Doering；Michael Ciesielski；Bettina Burk
申请人:Krems Chemie Chemical Services Ag；
IPC主号:

专利说明:

compounds which are effective as flame retardants.
Phosphorus compounds have long been known as flame retardants. Of these, in recent years, 9,10-dihydro-9-oxa-10-phosphaphen-anthren-10-one or oxide (DOPO), which was first developed by Sanko Chemical Co. Ltd. in DE 20 34 887, and various derivatives thereof. Their flame retardancy appears to be due to releasing phosphorus-containing radicals upon heating (see, e.g., Schafer et al., J. Appl Polym., 105 (2), 685-696 (2007)).
DOPO
Also, derivatives of diphenylphosphine oxide (DPhPO) and diphenyl phosphite (DPhOPO) are known as phosphorus compounds having flame retardancy and similar mechanism of action. O
diphenyl
diphenylphosphine
On the other hand, melamine and guanamine derivatives are among the known nitrogen-containing compounds with flame retardancy,
Melamine guanamine -1 - 2/24 • · · · · · ········· < Therefore, attempts have been made to combine such phosphorus-containing and nitrogen-containing compounds in flame retardants. Attempts have also been made to produce covalent bonds between such molecular groups.
In US 2003/120021 A1, US 6,797,821 B2, and US 2005/0004339 A1 by Wang et al. there are described curing agents for epoxy resins or epoxy resins cured therewith, each containing one or more DOPO or diarylphosphine oxide groups covalently bound to nitrogen-containing molecules, including melamine, methyl- and phenylguanamine, and having the formula:
R
N%
NtHyQ'jj
Therein, Q 'may inter alia be a DOPO or DPhPO radical, R may be NH2, CH3 or phenyl, and i and j are each 0, 1 or 2. However, in synthesis examples 13 and 14 of both applications cited only Products of the above formula in which i = 1 and j = 0, that is to say simply phosphorylated melamine or guanamine, by reaction of 1 mol of DOPO-CI, ie 10-chloro-9,10-dihydro-9-oxa-10-phosphaphenanthren-10-one, or 1 mol DPhPO-CI, i. Diphenyl phosphoryl chloride, with 1 mol of melamine with heating to about 170 ° C. General mention is also made of the analogous synthesis of compounds having more than one phosphorus-containing DOPO or DPhPO group by reacting i + 1 mol of Q'Cl with 1 mol of melamine or guanamine, but without specifying a specific process.
The inventors have discovered in the course of their research that this analogous reaction of up to 4 moles of DOPOCl or DPhPOCl with 1 mol of melamine or guanamine can not lead to the desired products if i and / or j = 2 (s), and especially not if melamine is to be derivatized only on two of its three amino groups. Because of the inertness of the hydrogen of an already easily derivatized with the respective phosphorus compound amino group, ie a group -NHQ ', namely, it can not even theoretically succeed in replacing one amino group twice with Q', without the hydrogens of the third -2-
more reactive than -NHQ '.
In addition, the method of Wang et al. very long reaction times. For example, stirring times of 16 h (for DOPO-CI) or 10 h (for DPhPO-CI) are required after complete addition of all reagents in order to achieve essentially complete conversion, although the reaction is carried out at temperatures of about 170 ° C ,
The aim of the invention was therefore to provide an improved process for the preparation of such or similar compounds, by means of which these compounds are obtainable in good yields, after relatively short reaction times and substantially without interfering side reactions.
DISCLOSURE OF THE INVENTION
This object is achieved by the invention by providing a process for the preparation of compounds of the following formula (I)
(0 in which - the radical R1 is selected from -NH2, -NH2.ZAZ and monovalent alkyl and aryl radicals, - the radicals A are each independently selected from the following phosphoryl radicals DOPO-, DPhPO- and DPhOPO- o
DOPO-DPhPO-DPhOPO- and
wherein at least one of the indices Φ 0;
in a first stage melamine or, when R1 is an alkyl or aryl radical, the corresponding alkyl- or arylguanamine with one or more of the following phosphinyl chlorides DOP-CI, DPhP-CI and DPhOP-CI ci I CI o-p
DOP-CI DPhP-CI DPhOP-CI is reacted to attach one or more phosphinyl residues to the amino group (s) of the melamine or guanamine, followed in a second step by the bound phosphinyl residue (s) by reaction with an oxidizing agent is oxidized to the / the corresponding phosphoryl radical (s) / are.
More specifically, in the first stage, a compound of the formula (II)
(H) wherein R2 is selected from -NH2 and monovalent alkyl and aryl radicals, i. Melamine or a guanamine, having one or more of the phosphinyl chlorides DOP-CI, DPhP-CI and DPhOP-CI converted to one or more compounds of the following formula (III) wherein:
R
(III) -4- 5/24 * are each independently selected from the following phos-phinyl residues DOP, DPhP and DPhOP-
the indices x, y, and z are as previously defined; then, in the second stage, the compound (s) of formula (III) is oxidized to one or more compounds of formula (I) by reaction with the oxidizing agent.
Not only can compounds of the formula (I) be prepared in good yields and essentially without side reactions, but it is also possible to prepare threefold-substituted melamines with the particular phosphorus-containing radical, and it is also very specifically mixtures of easily and doubly substituted aminotriazines available, as the later examples clearly show. In addition, the reaction times compared to the method of Wang et al. be significantly shortened, which represents a significant economic advantage, especially in view of the high reaction temperatures.
Without wishing to be bound by any particular theory, it is believed that this is attributable to the significantly higher reactivity of the phosphinyl chlorides compared to the corresponding phosphoryl chlorides. However, the almost quantitative yields in the preparation of the desired compounds were surprising. Precisely because of the high reactivity of the phosphinyl chlorides, it would actually be assumed that side reactions are more likely - especially at the preferred high reaction temperatures of up to 200.degree. That is, it was not to be expected that essentially exclusively the respective desired -5-6 / 24
I ·························································
Product is formed with one phosphorus-containing radical per amino group, but rather that in addition to a certain - albeit less - share arises with two phosphorus-containing radicals on an amino group. However, this was never observed. Thus, the phosphinyl chlorides used in the process according to the invention have sufficiently high reactivity to allow a rapid connection of exactly one phosphorus-containing group per amino group, but not sufficient to substitute the amino groups twice, even if a molar excess of the phosphinyl chlorides is used.
Furthermore, the phosphinyl chloride DOP-CI used in the process according to the invention for the preparation of DOPO Deriva th is an industrial intermediate in the production of the common flame retardant DOPO, is therefore produced in large quantities and is therefore much cheaper and easier to obtain than the phosphoryl chloride DOPO -CI used in the process of Chun-Shan Wang.
The monovalent alkyl and aryl radicals as options of the radicals R1 to R3 are preferably -CH3 or -ββΗ5, ie methyl or phenyl, since these are common and readily available guanamines - methylguanamine and phenyl or benzoguanamine - form. However, the process according to the invention is applicable to a wide range of substituents on the diaminotriazine nucleus and therefore the scope of protection should not be limited to these two preferred radicals.
The phosphorus-containing intermediates obtained in the first stage are largely stable to hydrolysis and can therefore easily be isolated, e.g. by stirring in water. However, one-pot reactions are possible for both stages. Both will be documented in the later embodiments.
The oxidizing agent is not particularly limited as long as it does not lead to undesirable side reactions of the reactants. In preferred embodiments, however, a peroxide is used, since any surpluses are easy to separate or destroy. In addition to hydrogen peroxide, H 2 O 2, numerous other peroxides and hydroperoxides come into question. Also the literature known -6-7 / 24 • *
Oxidation of DOP to DOPO with ozone is possible, but gave less good results than hydrogen peroxide or t-butyl hydroperoxide in the experiments of the inventors. The latter is to be preferred because of its higher stability and therefore easier handling over H2O2.
Since HCl liberates in the reaction between phosphinyl chloride and the aminotriazine, the first step is preferably carried out in the presence of an acid scavenger to shift the reaction equilibrium towards the product side. The acid scavenger is preferably 1-methylimidazole, although other compounds known to those skilled in the art are also suitable, such as ammonia, alkyl and aryl amines, and other nitrogen compounds, e.g. Triethylamine, pyridine, imidazole and the like, or other bases, e.g. Alkali and alkaline earth metal compounds. 1-Methylimidazole has the great advantage that its hydrochloride melts even at 75 ° C (while, for example, the non-methylated homologous imidazolium has a melting point of 158-161 ° C) and therefore with a suitable choice of the solvent and the reaction temperature, a second liquid phase in addition to Reaction solution forms, which is easy to separate.
Both stages are preferably carried out in an organic solvent to ensure the homogeneity of the reaction and the heat removal. The solvent is not particularly limited as long as it is chemically inert to the reactions occurring therein and the starting materials are soluble therein or at least dispersible. However, in the first stage, it should have a boiling point well above 75 ° C for the above reasons, have sufficiently good dissolving power for DOP-CI, and does not dissolve 1-methylimidazolium chloride. In the present invention, therefore, it is preferred to use a relatively non-polar, anhydrous solvent, more preferably an aromatic hydrocarbon, e.g. Benzene, toluene, xylene, etc., in particular toluene, used. Preferably, the same solvent is used both for the reaction of the aminotriazine with the phosphinyl chloride and for the subsequent oxidation. However, different solvents may be used, for example, chloroform for the first stage and toluene for the oxidation, etc. -7-8 / 24
In preferred embodiments of the invention * acts in the first stage of the acid scavenger simultaneously as a solvent, which is why here in particular 1-methylimidazole is used both as an acid scavenger and as a solvent. In the second stage chloroform or toluene, due to the absence of halogen, in particular toluene are preferred.
Although the invention is not limited thereto, it has been found in the research of the inventors that the first stage should preferably be carried out at a temperature in the range of 100 to 200 ° C to ensure short reaction times, high conversions and good yields. Similarly, temperatures in the range of 50 to 100 ° C have been found to be advantageous for the second stage.
Of course, the scope of the invention also includes the immediate process products of the process according to the invention, i. the compounds of formula (I) thus prepared.
Since the trisubstituted melamine, i. 10,2,4,6-Tris (9,10-dihydro-9-oxa-10-oxo-10-phosphaphenanthrene-10-ylamino) -1,3,5-triazine (DOP03-Mel): DOPOv
N
NH
N
DOPO ^ 'N N
N H
DOPO
H (DOPO) 3-Mel 0-P = 0
wherein DOPO- the radical y v-y corresponds, represents a new chemical connec tion, another aspect of the invention in the substance protection for this product and in its use as a flame retardant. In first fire - 8-9 / 24
Flame retardants for plastics, in particular for polystyrene and epoxides. EXAMPLES
The invention will now be described in detail by way of non-limiting embodiments.
example 1
Preparation of D0P03 Mel, i. 2,4,6-tris (9,10-dihydro-9-oxa-10-oxo-10-phospha-phenanthrene-10-ylamino) -1,3,5-triazine:
Stage 1 - Preparation of DOP3 Mel, i. 2,4,6-tris (9,10-dihydro-9-oxa-10-phospha-phenanthrene-10-ylamino) -1,3,5-triazine:
Melamine DOP-CI DOP3-Mel
An argon-filled 500 ml, 3-neck round bottom flask equipped with an internal thermometer, dropping funnel, stirrer, and inert gas transfer was -9-10 / 24
filled as acid scavenger and solvent and heated to 100 ° C. Thereafter, 72.4 g (0.31 mol) of DOP-CI were melted at about 100 ° C under inert conditions and filled into the dropping funnel. The DOP-CI was added dropwise with vigorous stirring over 1 h at 100 ° C, the dropping funnel was heated with a Heißluftföhn to avoid solidification of the reagent. The mixture was then stirred for a further 15 hours at 100 ° C. under argon, after which the viscous contents of the flask were stirred into 500 ml of water and the precipitated granular solid was filtered off with a glass frit. The filter cake was then slurried twice in 250 ml of water and filtered again. Subsequently, the substance was washed thoroughly with 200 ml of acetone and finally rinsed with n-pentane. After drying in air flow, 72.4 g (DOP) of 3-Mel were obtained in quantitative yield. 31P-NMR (101 MHz, DMSO-d6): δ 66.2; 66.1; 65.9 ppm. 1 H NMR (250 MHz, DMSO-d 6): δ 8.7-8.5 (d, 3 H, 3 NH-P); 8.25-8.15 (d, 6H); 7.68-7.53 (t, 6H); 7.50-7.40 (t, 3H), 7.38-7.28 (t, 3H), 7.27-7.17 (t, 3H), 7.08-6.97 ppm (m, 3H).
Step 2 - Oxidation of DOP3-Mel to DOP03-Mel
DOP3 mel DOP03 mel
In a 1-L three-necked flask equipped with a stirrer, internal thermometer and dropping funnel, the (DOP) 3-Mel (72.4 g) prepared in Step 1 was stirred at 50 ° C in 500 ml of chloroform, one part of which was dissolved , Subsequently, the mixture was cooled with a cooling bath to about 12 ° C and immediately started with the addition of an 11% solution of H2O2 (106.5 g, 34 mol) in ethyl acetate. The
temperature was maintained at about 15 ° C. Then the cooling bath was removed and stirring continued for a further 2 hours. Anhydrous sodium sulfate was added to the resulting turbid solution to separate the water formed in the reaction. After filtering off the drying agent, the product solution was concentrated at 40 ° C in a partial vacuum, wherein a tough substance said goodbye. After cooling to about 0 ° C was decanted. The residual solid was gradually heated to 230 ° C in vacuo. After about 30 minutes at this temperature, cooling and crushing of the crude product thus obtained, this was dissolved in 150 ml of chloroform. This solution was added dropwise with vigorous stirring in 500 ml of diethyl ether, wherein a white, granular solid separated, which was filtered off, washed with diethyl ether and dried at 60 ° C in vacuo. In this way, 67 g (DOPO) of 3-Mel were obtained (87.2% of theory). 31P-NMR (101 MHz, DMSO-de): δ 6.86; 6.67; 6.30 ppm. 1H-NMR (250 MHz, DMSO-d6): δ 9.9-9.3 (3H, 3NH-P); 8.40-8.22 (m, 3H); 8.18-8.00 (t, 6H); 7.78-7.58 (t, 3H), 7.55-7.35 (d, 6H), 7.35-7.16 ppm (m, 6H).
Elemental analysis for C39H27N6P3O6 (768.59 g / mol) calc .: C, 60.95; H 3.54; N, 10.93; Found: C 60.52, H 3.71, N 10.80.
Example 2
Preparation of D0P02-PhGuanamine, i. 2,4-bis (9,10-dihydro-9-oxa-10-oxo-10-phosphaphenanthrene-10-ylamino) -6-phenyl-1,3,5-triazine:
-11 -12 / 24 • ♦ «· ♦ * · · ·
Step 1 - Preparation of DOP2-PhGuanamine from Phenylguanamine and DOP-CI
A 3-necked flask filled with argon and equipped with a reflux condenser, stirrer and dropping funnel was charged with 6-phenyl-1,3,5-triazine-2,4-diamine (phenylguanamine, 33.1 g, 0.177 mol, 1 eq) and 1- Methylimidazole (145 g, 1.77 mol, 10 eq.) Filled. Then 91.2 g (0.389 mol, 2.2 eq.) DOP-CI were melted at about 100 ° C under inert conditions and filled into the dropping funnel. The DOP-CI was added dropwise with vigorous stirring over 1 h at 100 ° C, using a Heißluftföhn to keep it liquid. The reaction mixture was kept for a further 2 hours at this temperature and then stirred into 800 ml of distilled water. The precipitated solid was filtered off and washed 3 times with water and with acetone. Then, the crude product was stirred for 2 hours in 300 ml of boiling toluene. The still hot suspension was filtered and the isolated solid was washed thoroughly with toluene and finally dried in a stream of air. Thus, 97.24 g (0.1668 mol, 94.2% of theory) of (DOP) 2-PhGuanamine were obtained as a white solid.
M.p .: 276-282 ° C (toluene) 31P-NMR (101 MHz, DMSO-d6): δ 67.2 ppm (d, J = 19.5 Hz, 2P). 13 C-NMR (63 MHz, DMSO-de): δ 170.5 (m, 1C, Tr), 167.5 (m, 1C, Tr), 167.2 (m, 1C, Tr), 149.0 ( d, J = 2.4Hz, 1C), 148.8 (d, J = 2.3Hz, 1C), 135.5 (s, 1C, Ph), 133.0 (t, J = 2.2 Hz, 2C), 132.2 (s, 1C, Ph), 131.4 (s, 2C), 130.9 (d, J = 49.2 Hz, 2C-P), 130.4 (m, 2C ), 129.5 (s, 2C), 128.4 (s, 2C, Ph), 128.0 (s, 2C, Ph), 127.4 (d, J = 13.3 Hz, 2C), 125 , 6 (s, 2C), 123.8 (s, 2C), 123.5 (d, J = 5.7Hz, 2C), 123.4 (s, 2C), 120.5ppm (s, 2C ). 1 H-NMR (250 MHz, DMSO-d6): δ 8.97 (<jf, * J = 9.7 Hz, 2H) , 2NH-P), 8.35 (d, J = 6.8 Hz, 2H), 8.12 (d, J = 7.7 Hz, 4H), 7.73-7.63 (m, 4H) , 7.63-7.47 (m, 5H), 7.39-7.17 (m, 4H), 7.06 ppm (d, J = 6.4Hz, 2H). IR (KBr): v 206 (m, NH), 1540 (vs, 0 = CNH), 1506, 1486, 1424 (vs, P-Ph), 1197 (m, PO)
Ph), 1103, 943, 845, 879, 764 and 746 (s, C-H bend). HRMS (El) calcd for [12C33H23N5P202] +: 583.1327, found: 583.1379 [M] +. Elemental analysis for C33H23N5P202 (583.52 g / mol) calc .: C, 67.93, H, 3.97, N, 12.00, P, 10.62%; Found: C, 67.90, H, 3.93, N, 12.13, P, 10.64%.
Step 2 - Oxidation of DOP2-PhGuanamine to DOP02-PhGuanamine
DOP2-PhGuanamine D0P02-PhGuanamine
Into a three-necked flask equipped with reflux condenser, stirrer, thermometer and dropping funnel, 11.68 g (0.0020 mol, 1 equiv.) Of (DOP) 2-PhGuanamine in 50 ml of chloroform was heated to 40 ° C. After 15 minutes, the mixture was cooled to about 20 ° C with a cooling bath. Then 2.88 g (0.048 mol, 2.2 equiv.) Of a 30% strength aqueous solution of tert-butyl hydroperoxide were slowly added dropwise with vigorous stirring. Stirring was continued for 1 h, after which an additional 2.00 g (0.033 mol, 1.5 eq.) Of the oxidizer was added dropwise. The mixture was then stirred for a further 1 h at room temperature and the mixture was subsequently filtered. The isolated solid was washed with acetone. An additional fraction of the product was obtained by concentrating the residual solution in vacuo. The combined fractions were slurried in acetone with vigorous stirring, the suspension was filtered and the solid was dried in a stream of air. In this way, 11.75 g (0.0019 mol, 95.0% of theory) of (DOPO) 2-PhGuanamine were obtained as a white powder. -13-14 / 24
Mp: 267-273 ° C (dec.) ..... 31P-NMR (101 MHz, DMSO-d6): 8 6.8 (s, 1P), 6.7 ppm (s, 1P). 13 C-NMR (63 MHz, DMSO-d6): δ 170.3 (s, 1C, Tr), 165.2 (t, J = 3.5 Hz, 2C, Tr), 149.7 (d, J = 7.4 Hz, 1C), 149.6 (d, J = 7.5 Hz, 1C), 135.5 (d, J = 7.3 Hz, 2C), 134.1 (s, 1C, Ph) , 133.1 (d, J - 0.9 Hz, 2C), 132.1 (s, 1C, Ph), 130.5 (s, 2C), 130.3 (m, 2C), 128.5 ( d, J = 15.1 Hz, 2C), 127.8 (s, 2C, Ph), 127.7 (s, 2C, Ph), 125.2 (s, 2C), 124.5 (s, 2C), 123.8 (d, J = 164.3 Hz, 1C-P), 123.7 (d, J = 164.3 Hz, 1C-P), 123.5 (d, J = 11.5 Hz, 2C ), 120.9 (d, J = 12.0 Hz, 1C), 120.8 (d, J = 12.2 Hz, 1C), 120.0 ppm (m, 2C). 1H-NMR (250 MHz, DMSO-de): δ 10.39 (t, J = 8.0 Hz, 2H, 2NH-P), 8.36-8.28 (m, 4H), 8.11 7.88 (m, 2H), 7.70 (t, J = 7.4Hz, 2H), 7.57-7.16 (m, 9H), 7.07-6.87 ppm (m, 4H ). IR (KBr): v 3179 (w, NH), 1587 (C = C), 1538 (vs, 0 = CNH), 1493, 1454, 1417 (vs, P-Ph), 1232 (s, P = 0) , 1205 (s, PO-Ph), 1119, 1088, 943, 876, 751 and 785 (s, CH bend). HRMS (El) calcd for [12C33H23N5P204] +: 615.1225, found: 615.1220 [M] +.
Elemental analysis for C33H23N5P204 (615.51 g / mol) calc .: C, 64.39, H, 3.77, N, 11.38, P, 10.06%; Found: C, 64.07, H, 3.78, N, 11.25, P, 10.16%.
Example 3
Production of DOPO-Mel and DOPCVMel
Stage 1 - Preparation of DOP-Mel and DOP2-Mel
Into an argon-filled 250 ml three-necked round bottom flask equipped with an internal thermometer, dropping funnel, stirrer and inert gas transfer were added 6.31 g (0.050 mol) of melamine and 50 g (about 0.6 mol) of anhydrous 1-methylimidazole -14-15 / 24 ······· # ······················· «. ·· «« * »« Ι · ν · * · «** ····· *. filled and heated to 100 ° C. Then, 17.6 g (0.075 mol) of DOP-CI was melted at 100 ° C under inert conditions and filled in the dropping funnel. The DOP-CI was added dropwise with vigorous stirring over 45 minutes at 100 ° C using a Heißluftföhn to keep it liquid. After completion of the dropping, it was stirred at 120 ° C for 3 hours and then at 145 ° C for 1 hour. The 31P-NMR spectrum of the solution thus obtained showed that DOP-Mel and (DOP) 2-Mel were formed as reaction products. This solution was used after cooling to about 60 ° C without workup in the second stage.
Stage 2 - Oxidation of DOP-Mel and DOP2-Mel to DOPO-Mel and DOPÜ2-Mel
To the mixture of DOP-Mel and (DOP) 2-Mel in 1-methylimidazole obtained in step 1, 20 g (about 0.08 mol) of an about 37% toluene solution of tert-butyl hydroperoxide at 60 Dropwise at -65 ° C within 45 min with stirring. After completion of the addition of the reagent, the temperature was maintained at about 70 ° C for 2 hours. Then, the reaction mixture was stirred in 300 ml of water at a temperature of 50 ° C. After cooling, it was decanted. The substance thus obtained was dried for 15 hours in a stream of air, comminuted in a mortar and then stirred for 20 minutes in 300 ml of ethanol under reflux. After cooling to about 50 ° C was filtered and the solid pre-dried at 90 ° C in vacuo. Finally, it was heated to 170 ° C. in a vacuum drying oven for about 10 hours (pressure about 12 mbar). The 1H and 31P NMR spectra of the product showed a total content of about 98% of DOPO-Mel and (DOPO) 2-Mel in a molar ratio of about 1: 1. 31P-NMR (101 MHz, DMSO-d6): δ 8.79 ppm (DOPO-Mel); 7.60; 7.42 ppm ((DOPO) 2-Mel). 1 H NMR (250 MHz, DMSO-d 6): δ 9.8-9.1 (NH-P); 8.15 to 8.03; 7.8-7.6; 7.55-7.45; 7.45-7.25; 7.25 to 7.2; 6.8-5.7 (NH2). MS (ESI): 341 (DOPO-Mel, M + 1); 555 ((DOPO) 2-Mel, M + 1). - 15-16 / 24 * ♦ -
Example 4
Preparation of DPhP02-PhGuanamine, i. 2,4-bis (diphenylphosphoryl) -6-phenyl-1,3,5-triazine:
Step 1 - Preparation of DPhP2-PhGuanamine from phenylguanamine and DPhP-CI
DPhP-CI DPhP2-PhGuanamine
PhGuanamin
Into an argon-filled three-necked flask equipped with reflux condenser, thermometer, stirrer and a dropping funnel were added phenylguanamine (2.38 g, 0.0127 mol, 1 eq), 1-methylimidazole (2.29 g, 0.0279 mol , 2.2 eq.) And 40 ml of anhydrous toluene and heated to 80 ° C. At this temperature, 6.16 g (0.0279 mol, 2.2 equiv.) Of diphenylphosphinyl chloride (DPHP-Cl) were slowly added dropwise with stirring. Thereafter, the now biphasic reaction mixture was stirred at 90 ° C for 2 h. Thereafter, the upper phase was decanted under inert conditions from the viscous body of soil (1-Methylimidazoliumchlorid) and thereby transferred via a connecting piece in a second, also filled with argon three-necked flask. In this way, a solution of DPhP2-PhGuanamin was obtained, which was used without work-up in the second stage. -16-17 / 24 w »τ *» w «·
Step 2 - Oxidation of DPhP2-PhGuanamine to * DFihPC32-PhGuanamine
DPhP2-PhGuanamine DPhP02-PhGuanamine
The three-necked flask with the DPhP2-PhGuanamine solution prepared in Step 1 was fitted with a reflux condenser, thermometer, stirrer and dropping funnel charged with 6.86 g (0.0381 mol, 3 equiv.) Of an 11% solution of H2O2 in Ethyl acetate was filled. Then, the reaction mixture was cooled to about 5 ° C with an ice water bath and the oxidizing agent was added dropwise slowly and with vigorous stirring, the temperature was kept at a maximum of 15 ° C. Upon completion of H 2 O 2 addition, the cooling bath was removed and the reaction mixture stirred for a further 15 h. The precipitated solid was filtered off, washed with toluene and then stirred for 1.5 hours in 50 ml of boiling toluene. The hot suspension was then filtered and the solid was washed again with toluene and finally dried in vacuo (20h, 150 ° C). In this way 5.64 g (0.0096 mol, 75.6% of theory) of DPhPO 2-PhGuanamine were obtained as a white solid. 31P-NMR (101 MHz, DMSO-de): δ 16.1 ppm. 1H-NMR (250 MHz, DMSO-d6): 6.9.89 (d, J = 10.2 Hz, 2H, 2NH), 7.85 (m, 8H), 7.50 ppm (m, 14H), 7.15 ppm (m, 3H). HRMS (El) calcd for [12C33H27N5P202] +: 586.1562; Found: 586.1656 [M-H] +.
Example 5 - Measurements of flame retardancy
An Epoxynovolak, D.E.N. 438 from Dow Chemicals with an EEW (epoxy-eequivalent lent weight) of 179 g / mol was mixed with 0.1 wt% triethanolamine and the new -17-18 / 24 »«
Compound of the invention, D0P03-Mel, as a flame retardant additive - mixed in the amount necessary in each case for setting the required phosphorus content in the test specimen. The mixture was then held for 2 hours at 140 ° C, degassed by vacuum and cooled to 90 ° C. The preformulation thus prepared was mixed at 90 ° C with 6 parts by weight of dicyandiamide and 2 parts by weight of fenuron, based on 100 parts by weight of Epoxynovolak. Curing was carried out in an aluminum dish by gently heating to 120 ° C within 30 minutes, holding this temperature for 1 hour, raising the temperature to 130 ° C for 1 hour and then holding a temperature of 200 ° C for 2 hours. From this specimens were molded with 70 x 13 x 4 mm and classified to characterize the fire properties according to UL94.
UL94 is the test specification of Underwriters Laboratories, which has been incorporated into IEC / DIN EN 60695-11-10 and -20 with the same content. In this case, ignition flames with a power of 50 W act twice briefly on the sample body, wherein the vertical test, the burning time and the falling of burning parts are evaluated using a arranged below the sample body Wattebausche. The classification takes place in the stages "V0", "VT" and "V2H", which are explained in Table 1 below:
Table 1: UL94 classification
Classification of V1 V2 post-combustion time after each flame &lt; 10 s &lt; 30 s &lt; 30 s total burning time per set (10 flames) &lt; 50 s &lt; 250 s &lt; 250 s afterburn time / afterglow after 2nd flame &lt; 30 s &lt; 60 s &lt; 60 s Burn-off to holding chamber no no no Ignition of cotton wool no no yes
The classification &quot; V0 &quot; therefore represents the highest requirement for fire protection and is therefore desirable in the use of flame retardant compositions. -18-19 / 24 • · · · · ············· ·
Table 2 below shows the results of the test for DOPCVMel and for DOPO as reference substance.
Table 2
Flame Retardant Additive Phosphorus Content (wt%) UL94 Classification - 0.0 unclassified Comp: DOPO 1.0 unclassified Comp: DOPO 1.4 V1 Comp: DOPO 1.6 VO Comp .: DOPOg Mel 1, 0 V1 Experience: DOPOg-Mel 1.4 VO
From these results clearly shows an improved flame retardancy of DOPCVMel over the commercial additive DOPO. Thus, the new compound D0P03-Mel is very well suited as a flame retardant in plastics. -19- 20/24

权利要求:
Claims (12)
[1]
PATENT REQUIREMENTS Process for the preparation of compounds of the following formula (I) R 1 N 1 N 2 O. X'NH 2 .yAy (1) where - the radical R1 is selected from -NH2, -NH2-ZAZ and monovalent alkyl and aryl radicals, - the radicals A are each independently selected from the following phosphoryl radicals DOPO-, DPhPO- and DPhOPO-

DOPO-DPhPO-DPhOPO- and - the indices x, y, and z are each independently 0 or 1, with at least one of the indices Φ 0; in a first step, melamine or, when R1 is an alkyl or aryl radical, the corresponding alkyl or arylguanamine with one or more of the following phosphinyl chlorides DOP-CI, DPhP-CI and DPhOP-CI

reacting one or more phosphinyl radical (s) with the amino group (s) of the melamine or guanamine, and then in a second step the bound phosphinyl radical (s) to the corresponding phosphoryl radical (s) by reaction with an oxidizing agent ( en) is / are oxidized. -21 -21/24 ········································································. ··
[2]
2. The method according to claim 1, characterized in that the monovalent alkyl or aryl radical of R1 is selected from -CH3 and -C6H5.
[3]
3. The method according to claim 1 or 2, characterized in that a peroxide is used as the oxidizing agent.
[4]
4. The method according to claim 3, characterized in that hydrogen peroxide or t-butyl hydroperoxide is used as the oxidizing agent.
[5]
5. The method according to any one of the preceding claims, characterized in that the first stage is carried out in the presence of an acid scavenger.
[6]
6. The method according to claim 5, characterized in that the acid scavenger simultaneously acts as a solvent.
[7]
7. The method according to claim 6, characterized in that 1-methylimidazole is used as acid scavenger and solvent.
[8]
8. The method according to any one of the preceding claims, characterized in that the second stage is carried out in an organic solvent selected from chloroform and toluene.
[9]
9. The method according to any one of the preceding claims, characterized in that the first stage is carried out at a temperature in the range of 100 to 200 ° C.
[10]
10. The method according to any one of the preceding claims, characterized in that the second stage is carried out at a temperature in the range of 50 to 100 ° C.
[11]
11. 2,4,6-tris (9,10-dihydro-9-oxa-10-oxo-10-phosphaphenanthren-10-ylamino) -1,3,5-triazine (D0P03-Mel): -22- ···························: ·. ·· · :. · · · · · · · # * * «* ·· ·· ·· ···· · DOPCk NH N ^ N DOPOv. / W JK ^ DOPO N N N Η H where DOPO- the rest

equivalent.
[12]
12. Use of 2,4,6-tris (9,10-dihydro-9-oxa-10-oxo-10-phosphaphenan-thren-10-ylamino) -1,3,5-triazine as a flame retardant. Vienna, August 29, 2012 Krems Chemie Chemical Services AG -23- 23/24

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同族专利:

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公开号 | 公开日

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EP2890702B1|2016-08-24|

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AT513327B1|2014-06-15|

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KR20150052138A|2015-05-13|

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US9238777B2|2016-01-19|

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JP2015530999A|2015-10-29|

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DK2890702T3|2016-12-19|

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EP2890702A1|2015-07-08|

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US20150203759A1|2015-07-23|

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RU2639161C2|2017-12-20|

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WO2014032070A1|2014-03-06|

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RU2015110993A|2016-10-20|

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CN102190801B|2011-03-29|2012-11-21|湖南科技大学|Preparation method for nonionic oxidized polyethylene wax emulsion using single emulsifier|CN106633052B|2015-11-04|2019-06-25|华中师范大学|Phospho hetero phenanthrene-triazine difunctional oligomer and preparation method thereof and fire-retardant application|

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CN105541917B|2016-01-27|2017-10-17|厦门大学|A kind of phosphorus nitrogen collaboration polyester flame-retardant agent and preparation method thereof|

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KR102054675B1|2017-06-20|2019-12-11|엔나노텍|flame-retardant ester polyol, the manufacturing method thereof and polyisocyanurates including the anti-flame ester polyol|

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法律状态:
2014-12-15| PC| Change of the owner|Owner name: METADYNEA AUSTRIA GMBH, AT Effective date: 20141107 |

优先权:

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申请号 | 申请日 | 专利标题

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ATA944/2012A|AT513327B1|2012-08-29|2012-08-29|Process for the preparation of phosphorus-containing compounds|ATA944/2012A| AT513327B1|2012-08-29|2012-08-29|Process for the preparation of phosphorus-containing compounds|

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RU2015110993A| RU2639161C2|2012-08-29|2013-08-28|Method of producing phosphorus-containing flame retardants|

---

JP2015528803A| JP2015530999A|2012-08-29|2013-08-28|Method for producing phosphorus-containing flame retardant|

---

PCT/AT2013/050167| WO2014032070A1|2012-08-29|2013-08-28|Method for producing phosphorus-containing flame retardants|

---

DK13780050.4T| DK2890702T3|2012-08-29|2013-08-28|A process for preparing phosphorus-containing flame retardants.|

---

EP13780050.4A| EP2890702B1|2012-08-29|2013-08-28|Method for producing phosphorus-containing flame retardants|

---

KR1020157007873A| KR20150052138A|2012-08-29|2013-08-28|Method for producing phosphorus-containing flame retardants|

---

US14/633,156| US9238777B2|2012-08-29|2015-02-27|Method for producing phosphorus-containing flame retardants|