Method for oxy- and methoxy derivatives of diphenylmethane preparation

专利摘要:
The mutual condensation of aromatic and carbonylic compounds is carried out with zeolitic materials derived from silicalite by replacing a portion of silicon with B and Al, Al and Ti, Ti and Fe, and with ZSM-5, to yield diaryl-alkanes.
公开号:SU1739843A3
申请号:SU874203612
申请日:1987-10-21
公开日:1992-06-07
发明作者:Габриэле Клеричи Марио；Белусси Джузеппе
申请人:Эниричерке С.П.А., Эникем Синтезис С.П.А., Снампрогетти С.П.А. (Фирма)；
IPC主号:

专利说明:

four.
with
This invention relates to organic chemistry and concerns a process for the preparation of hydroxy and methoxy derivatives of diphenylmethane.
A known method for producing hydroxy and methoxy derivatives of diphenylmethane by condensation of formaldehyde or trioxane with phenol or anisole in
the presence of a catalyst is a solid acid, for example crystalline aluminosilicate.
The closest technical solution to the present invention is the condensation of these compounds, catalyzed by zeolites of type X, Y and mordenite in acid form, or containing
Smhh metal from the group of lanthanides at elevated temperatures.
The disadvantage of this method is the low selectivity for the yield of the para-isomer, 4, V-dioxy- or dimethoxy-diphenylmethane in the mixture with b, k and 2, k -isomers, which does not exceed 29%.
The purpose of the invention is to increase the yield of the para-isomer.
For this purpose, it was proposed to use zeolites from silicates as a catalyst by replacing part with silicon with boron and aluminum, aluminum and titanium, titanium and iron, as well as zeolite ZSM-5. The reaction is carried out in a suitable inert solvent, which dissolves the reacting substances, and from room temperature to 200 ° C, preferably from 50 to 120 ° C, in batch or continuous mode, with separation of the reaction product and recirculation of unreacted substances. The pressure in the reactor is determined by the vapor pressure of the components at a given temperature. The catalyst is used in the form of microspheres with a diameter of 20 µm and contains one of zeolites A, B, C in pure form or in mixture with oligomeric silicon oxide and has a composition corresponding to the general pH formula A102-qBz03-Si02, where, 005-0.0032 and , 005-0.02 for zeolite A. pH A102qTi02-SiOz, where, 0073-0.0081 and, 0225-0.025 for zeolite B, pH F Oj-qTiOg-SiOj, where, 0025 and, 0188-0.0208 for zeolite C. Each of zeolites A, B, C has characteristic X-ray and diffraction and infrared spectra, respectively shown in Table. 1-3.
During the condensation of formaldehyde and phenol, the reaction is carried out in water at the boiling point and during the condensation of trioxane and phenol in benzene at 120 ° C.
An advantage of the invention is the high yield of the para-isomer (,), which is compared with a yield of 29% in the known process.
Example 1. Zeolite A is prepared according to a procedure common to all zeolites, including the following operations.
Under hydrothermal conditions, the reaction is carried out between the derivatives of silicon, boron, aluminum and the nitrogenous organic base in molar ratios Si02 / Al20i 100, preferably
-

 .
15
20
in the range from 300 to 00, U2 / Br03, possibly in the presence of one or more alkali or alkaline earth metal salts and / or hydroxides, with a molar ratio of M / Si02 (hereinafter M means alkali or alkaline earth metal cation) reactants less JQ than 0.1, preferably less than 0.01.
In the empirical formula of the catalyst, aluminum (hereinafter shown in the Form NAYU2, to emphasize that the material exists in the protonated form). If there is no specific indication of the relationship between the various reagents, the aluminum is used in the form A1gO, since this form is the most is common.
The silicon derivative is chosen from silica gel, silicasol and alkyl silicates, among the latter tetraethyl silicate is most preferable, boron derivative is chosen from boric acid and organic boron derivatives, such as alkyl borates, preferably triethylborate, aluminum derivatives are selected from its salts such as, for example, halo derivatives and hydroxides, as well as organic derivatives, such as alkyl aluminates, preferably isopropyl aluminate.
The nitrogen-containing organic compound may be an alkyl hydroxide, preferably tetrapropylammonium hydroxide, f
In the case of using tetrapropylammonium hydroxide (GTPA), the ratio TPA / S102 is in the range 0.1-1.0, preferably 0.2-0.
The reaction is carried out at 100-200 ° C, preferably 1bO-180 ° C, and a pH in the range of 5 to 9-1, preferably 10-12, for 1 hour to 5 days, preferably 3-10 hours.
Zeolite A is prepared as follows. 67.8 g of A1 (G).}} 3 9I20 dissolved
 in 1275 g of ethanol and to the solution thus obtained, add 2 819 g of tetraethyl silicate with stirring to obtain a homogeneous and transparent solution.
55 in a stainless steel reactor are placed under stirring in the specified order of 1036 g of deionized water, 8878 g of an aqueous solution of GTPA from the end of 30
167.5 g
concentration of 15.5 wt.% and boric acid boric acid.
After the boric acid is completely dissolved, the previously prepared solution is added to the solution and stirred at about 60 ° C for about 4 to complete the hydrolysis of silicon and the alcohol is almost completely removed. The molar ratio of components in the reaction mixture is SiO2 / Al203 150, SiOz / B20 10, TPA / Si02 0.5, HaO / SiO ,,.
The resulting solution is placed in an autoclave and heated under spontaneously developing pressure at k h. The discharged product is centrifuged and the precipitate taken out of the centrifuge is carefully dispersed in 70 l of deionized water, the resulting suspension is again centrifuged and a washed compacted precipitate is obtained.
;
4 A portion of this precipitate is calcined in air for 5 hours at 550 ° C. A zeolite is formed, the anhydrous form of which has the following composition, in mol x, with respect to Si02: 0.0098 A1203
0,0108, si ° 2. The obtained zeolite A has an x-ray diffraction spectrum (X-ray) and a PC spectrum given in Table. one.
Table 1
Radiograph of the flat plane - 11,12 + 0,10 tonne - 9,98 + 0,10. 9,, 10 (d), 1 6,, 07 5.97 + 0.07, 05 3,, 04 3.81 + 0.0 3.73 + 0.0 3.71 + 0, ( AND
h, bz + o, o4
3, 02 2.97 + 0.02
o.s.
with. Wed Wed.
with
-II- - -
P
Wed Wed.
Note. Hereinafter, to denote the intensity of contraction: s - strong, eaten. - weak, cf. - average, s.s. - between medium and strong, sr. - between medium and weak.
Example2. Receiving zeolite A with a binder.
Zeolite A is prepared as indicated in Example 1. Then, 219 g of tetraethyl silicate is added with vigorous stirring to a g of 12 wt.% GTPA solution and the reaction mixture is stirred for 1 h, then 958 ml of demineralized water is added to the mixture, and stirring is continued for another 1 hour. From the clear solution after hydrolysis, 875 g of sediment of the following composition are obtained, in May .: TPA 9, water 26, zeolite A 65.
The suspension with the consistency of milk, obtained from the dispersed mass, is fed to the spray dryer (Niro-Atomizer, disc spray dryer, leaving air temperature 120 ° С, chamber diameter 1.5 m) and get dense microspheres with an average diameter close to 20 microns.
The product is calcined at 550 ° C in a muffle furnace under a nitrogen atmosphere for 2 hours, and then the nitrogen is gradually replaced with air, and the product is additionally kept for 2 hours at 550 ° C in air.
The catalyst obtained has the following composition, in mol x, relative to Si02: 0.0088, 0.0097 Br03, SiOz.
PRI me R 3. Zeolite B is prepared according to the general procedure using the following operations.
Under hydrothermal conditions, the reaction is carried out between derivatives of silicon-titanium, aluminum and a nitrogen-containing organic base with a molar ratio of Si02 / Alz05 greater than 100, preferably 300-400, with a molar ratio of Si02 / Ti02 greater than 5, preferably V5-25, at a mole ratio of H20 / Si02, in the range of 10-100, preferably 30-50, possibly in the presence of one or more alkali and / or alkaline earth metal salts and / or hydroxides, at a molar ratio of M / Si02 (where cation of alkali and / or alkaline earth metal) less than 0.1, preferably Smaller, 0.01 "Derivatives of silicon are chosen from silica gel, silicasel and alkyl silicates, among which tetraethylsilicate is most preferable, the derivative of titanium is chosen from salts such as halide salts and organic derivatives of titanium, such as alkyl titanates , preferably tetraethyl titanate, aluminum derivatives are chosen among its salts, such as, for example, halide salts and hydroxides, as well as organic derivatives, such as, for example, alkyl aluminates, the desired distance (d), A
but isopropylaluminate. |
Nitrogen-containing organic base - Table 2
Alkyl ammonium hydroxide, preferably GTPA, may serve as the compound.
The ratio of FTPA / Si02 is chosen in the range of 0.1-1.0, preferably 0.2- 0.4.35
The reaction is carried out at 100-200 ° C and a pH in the range of 9-14, preferably 10-12, and the duration of the reaction is in the range from 1 hour to 5 days, preferably h. 40
Zeolite B is prepared as follows.
27 g of ammonium isopropoxide are dissolved in 5400 g of a GTPA solution with a concentration of 18.7 May D.
Separately, 230 g of tetraethyl orotbitanate is dissolved in 4160 g of tetraethyl silicate and this solution is added to the previous solution with stirring.
The resulting mixture is heated to 50-60 ° C with stirring until a homogeneous solution is obtained. 10 liters of water are then added.
The resulting solution is discharged into the autoclave 55 and heated at self-propelled, - freely generated pressure at l70 ° C for 4 h.
45
50
Roentgenogram
Interplanar-11.14 + 0.10 o.
9.99 + 0.10s
9.74 + 0.10sr.
6.36 + 0.07 sr.
5.99 + 0.07 sr.
4.26 + 0.05 sr.
3.86 + 0.04 s.
3.82 + 0.04 s.
3.75 + 0.04 s.
3.72 + 0.04 s.
3.65 + 0.04 sr.
3.05 + 0.02 sr.
2.99 + 0.02 sr. Infrared spectrum Wave number (Wft), cm
 I
1220-1230 1080-1110 960-975 795-805
ate with.
Wed. Wed.
0
five
five
The product discharged from the autoclave is centrifuged and washed twice with redispersion, then centrifuged. A part of the precipitate washed and tightly pressed in the centrifuge is calcined in air for 5 hours at 550 ° C until zeolite C is formed, which has the following composition in anhydrous form, in mole% relative to Si02: 0.0081 AL, 0.0250 T10g, 810g.
Radiograph and IR spectrum of zeolite B are given in table. 2
Example 4: Preparation of zeolite B with binder.
The zeolite was prepared according to Example 3 and then, with vigorous stirring, 320 g of tetraethyl silicate was added to 340 g of an aqueous solution of GTPA with a concentration of 12 May D. The resulting mixture was heated for 1 hour, then 1400 ml of demineralized water was added and the solution was kept stirring for another 1 hour.
The resulting clear solution contains 1280 g of carefully dispersed, washed, tightly pressed on the centrifuge sediment containing, in May.%:. TPA 9, water 26, zeolite B 65.
distance (d), A
0
five
five
0
Roentgenogram
Interplanar-11.14 + 0.10 o.
9.99 + 0.10s
9.74 + 0.10sr.
6.36 + 0.07 sr.
5.99 + 0.07 sr.
4.26 + 0.05 sr.
3.86 + 0.04 s.
3.82 + 0.04 s.
3.75 + 0.04 s.
3.72 + 0.04 s.
3.65 + 0.04 sr.
3.05 + 0.02 sr.
2.99 + 0.02 sr. Infrared spectrum Wave number (Wft), cm
 I
1220-1230 1080-1110 960-975 795-805
ate with.
Wed. Wed.
Continuation of table 2
Note. Only the main characteristic bands of zeolite B are given.
A suspension with the consistency of milk, obtained after dispersion, is fed to a spray dryer (see example 2). The resulting compact microspheres have an average diameter close to 20 μm.s
The product is loaded into a muffle furnace and heated to 550 ° C for 2 hours under a nitrogen atmosphere. Then, nitrogen is gradually displaced by air and the product is kept at 550 ° C for an additional 2 hours in air.
The resulting product has the following composition, in mol x, relative to 0.0073 A1Ј03, 0.0255 Ti02, Si (2.
Example 5. Preparation of zeolite C.
Under hydrothermal conditions, the derivatives of silicon, titanium, iron and the nitrogen-containing organic base react with a molar ratio greater than 50, preferably 150-600, with a molar ratio of SiO / Ti02 greater than 5, preferably with a molar ratio of HjO / SiOg in 10-100, preferably 30-50, possibly with one or more alkali or alkaline earth metal salts and / or hydroxides, with a molar ratio of M / SiO less than 0.1, preferably less than 0.08.
Hereinafter, in the empirical formula of the material, iron is shown in the form of HFe02 to emphasize that the material is in the H form. Unless otherwise indicated, iron is used in the form of Fe203, as the most commonly used.
The silicon derivative is selected from silica gel, silicasol and alkyl silicates, among which tetraethyl silicate is most preferable, titanium derivatives are chosen among salts, such as halide salts, and organic titanium derivatives, such as alkyl titanates, preferably tetraethyl titanate, iron derivative is chosen among its salts
t739843
ten
as, for example, halide salts or nitrates, hydroxides and organic derivatives, such as alkoxides, for example.
The nitrogen-containing organic base can be alkylammonium hydroxide, preferably GTPA.
In the case of the use of GTPA, the GTPA / SiO ratio is in the range of 0.1-1.0, preferably 0.2-0.4.
The reaction is carried out at 100-200 ° C.
preferably 1bO-180 ° C, at pH, it is 5 days in the range of 9-14, preferably 10-12, and for the period from 1 hour to 5 days, preferably 3-10 hours.
Titanium ferrosilicate is prepared as follows.
20.2 g of Fe (NOg) 3-9H20 are dissolved in water and the hydroxide is precipitated from the solution by the addition of ammonium hydrate. The precipitate is filtered, washed until neutral by re-dispersing in cold water and filtering until neutral. The moist hydroxide is then dissolved in 2700 g of GTPA with a concentration of 18.7% by weight.
Separately, 114 g of tetraethyl orthotitanate was dissolved in 2080 g of tetraethyl orthosilicate and this solution was added to the previous solution with stirring.
The resulting mixture is heated to 50-60 ° C with stirring until a homogeneous solution is obtained, then 5 L of water is added.
The solution obtained in this way is placed in an autoclave and heated at a spontaneously developing pressure at 170 ° C for 4 hours.
The product discharged from the autoclave is centrifuged and washed twice with the aid of redispersion and centrifugation. A part of the dense washed sediment pressed in a centrifuge is calcined in air for 4 hours at 550 ° C to form a zeolite having an anhydrous form, the following composition, in mole x 810g: 0.0025 Fe /, 0.0208 TiOg, Si02.
Radiograph and IR spectrum of the zeolite are given in table. 3
blitz 3
17398 3
ka ma
Example 6: Preparation of zeolite C with a binder.
The zeolite is prepared according to Example 5, then 162 g of tetraethyl silicate is added with vigorous stirring to 173 g of a solution of GTPA with a concentration of 12 wt.% And the mixture obtained is stirred for 1 h, 708 ml of demineralized water are added and the solution is stirred for another 1 h.
The clear solution thus obtained, in which 720 g of dense precipitates are carefully dispersed12
S
0
five
0
five
0
five
ka, pressed in a centrifuge, contains, masd: GTPA 9, water 2,6, zeolite C 65,;
 Suspension with milk consistency,
 obtained from the dispersion, served in a spray dryer (see example 2). The resulting contact microspheres have an average diameter close to 20 microns.
After the spray dryer, the product is placed in a muffle furnace with a nitrogen atmosphere and heated to 550 ° C for 2 hours. Then the nitrogen is gradually replaced with air and the product is left to stand for another 2 hours at 550 ° C in air.
The resulting product has the following composition, in mol x, 0.0025, 0.0188 TiCbz., Si02.
Example. Zeolite ZSM-5 is prepared according to a known method.
I Example 8-10. The following examples demonstrate the use of zeolites prepared according to examples 1-7 for the preparation of hydroxy and methoxy derivatives of diphenylmethane by condensation of phenol or anisole with formaldehyde.
2 g of the catalyst is suspended in a solution containing 8 g of phenol, 3 g of a 0% aqueous formaldehyde solution and 50 ml of water.
With stirring, the suspension is heated at boiling point for 6 hours, and the reaction mixture gradually becomes reddish. After removing the water, the residue is extracted with ethanol, subjected to quantitative analysis using gas chromatography and mass spectrometry analysis calibrated to the appropriate standards.
The results are shown in Table. . The major products are dioxidiphenylmethane (DODM) isomers. Higher oligomers are present in trace amounts.
Table k
13
- Example 11. Sg of zeolite B is suspended in a mixture of 20 g of anisole and 3 ml of 40% aqueous formaldehyde in 50 ml of a 50% aqueous solution of ethanol in water. The suspension is heated in an autoclave at 120 ° C for 4 hours.
The degree of conversion of anisole 35%. The main product is isomers of dimethoxyphenylmethane (DMFM). Isomer selectivity, g: 2.2 - 12, 2.4 - 15, 4.4 - 84. Higher oligomers are present as traces.
Example 12: 2 g of zeolite A, 12 g of phenol and 1.5 trioxane dissolved in 60 ml of benzene are introduced into a glass reactor.
The reaction mixture is heated at 120 ° C for 5 hours with magnetic stirring. After cooling, the solvent was distilled off and the residue was extracted with ethanol. The reaction products are analyzed by gas chromatography and mass spectrometry.
The degree of conversion of phenol is 65%. Selectivity for DMFM isomers, g: 2.2 - 1.2; 2.4 - 2.3; 4.4 - 4.1.
Example 13. 3.3 g of a catalyst of zeolite B with a binder are suspended in a solution of 20 g of anisole and 4 ml of 40% aqueous formaldehyde in 50 ml of a 50% solution of ethanol in water.
The suspension is heated in an autoclave at 120 ° C for 4 hours.
The degree of conversion of anisole 35%. Selectivity for DODM isomers, g: 2.2 - 1; 2.4 - 15; 4.4 - 84.
Higher oligomers are present only as traces.
Example 14. 12 g of phenol, 1.5 g of trioxane dissolved in 60 ml of benzene, together with 2.2 g of catalyst - zeolite A with a binder, are introduced into a glass reactor.
The reaction mixture was stirred at 120 ° C for 5 hours with a magnetic stirrer. The reaction products are analyzed by gas chromatography and mass spectrometry.
Phenol: conversion rate of 65%. Selectivity for DODI isomers, g; 2.2 - 1.2; 2.4 - 2.3; 4.4 - 4.1.
Example 15. 2.2 g of a zeolite C catalyst with a binder are suspended — in a solution of 8 g of phenol, 3 ml of a 40% aqueous formaldehyde solution and 50 ml of water. The suspension is heated with stirring at a temperature of 7739843
14
(
ten
15
nor 6 h, and the reaction mixture gradually becomes reddish. After removing the water, the residue is extracted with ethanol and analyzed by gas chromatography and mass spectrometry using pure samples as standards.
Phenol conversion 18%. Selectivity for DODM isomers, g: 2.2 - 3.5; 2.4 - 30, 4.4 / - 66.
The data presented in the examples show the possibility of selectively obtaining the para-isomer of the hydroxy and methoxy derivatives of diphenylmethane with a yield of 66-84%.

权利要求:
Claims (4)
[1]
1. A method for producing hydroxy- and methoxy-derivatives of diphenylmethane by condensation of phenol or anisole with formaldehyde or trioxane in an inert solvent at elevated temperatures in the presence of a zeolite catalyst, characterized in that, in order to increase the yield of the para-isomer, using a catalyst in the form of microspheres with a diameter of 20 μm, which contains zeolite ZSM-5 or one of zeolites A or B or C, corresponding to the general formula pJIA102. “XSi02, where, 005-0.032 and, 005-0.02 for zeolite A А pHAlOg.qTiO. SiOz, 5 where, 0073-0, 0081 and, 0225-0.025 for zeolite B, pHFajpC -qTiQ Si02, where, 0025 and, 0188-0.0208 for zeolite C, each of the zeolites having X-ray diffraction spectra and infrared spectra, shown in Tables 1, 2 and 3, respectively, and used in pure form or mixed with oligomeric silica.
[2]
2. A process according to claim 2, in which the solvent is water in the case where formaldehyde and phenol are the reactants and the reaction is carried out at boiling point.
[3]
3. A method according to claim 2, characterized in that the solvent is benzene when the reagents are trioxane and phenol, and the reaction is carried out at 120 ° C.
five
[4]
4. A method according to claim. Characterized in that the reaction is carried out at a pressure which develops as it flows.
0
0
five
0

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法律状态:

优先权:

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申请号 | 申请日 | 专利标题

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IT8622073A|IT1213366B|1986-10-22|1986-10-22|PROCEDURE FOR THE CONDENSATION BETWEEN AROMATIC AND CARBONYL COMPOUNDS.|

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