• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    An improved process for the preparation of asymmetrical N-phenyl-N'-substituted para-phenylene diamines by the reductive alkylation of para-nitroso-diphenylhydroxylamine with an aldehyde or a ketone in the presence of hydrogen and a hydrogenation catalyst is disclosed. The improvement comprises utilizing as the hydrogenation catalyst (1) one member selected the group consisting of palladium and platinum sulfide, in an amount less than 1%, by weight, based on the weight of para-nitroso-diphenylhydroxylamine, and (2) activated carbon with a specific surface area of at least 700 square meters per gram and an ash content of less than 7.5%, by weight.
    公开号:SU841580A3
    申请号:SU792750901
    申请日:1979-04-13
    公开日:1981-06-23
    发明作者:Бергфельд Манфред；Ценгель Ханс-Георг
    申请人:Акцо Н.В. (Фирма)；
    IPC主号:
    专利说明:

    (54) METHOD FOR OBTAINING NYSYMMETRIC N-PHENYL-N-SUBSTITUTED P-PHYLENEDIAMINES
    discontinuous modes. The reaction temperature and pressure in the reaction vessel are not so significant. The method is carried out at normal pressure and room temperature, however, due to the influence of pressure and temperature on the reaction rate, it is advisable to carry it out at elevated temperature and increased pressure. It is recommended that TC operate in a temperature range from 20 to. The reaction temperature is aS-laS C, preferably 40-100 ° C. The pressure of hydrogen can vary widely, for example in the range 1-150 bar. Its value is 5-15 bar, preferably 7-12 bar. The reaction time is 15 min - 5 hours, preferably 0.5-3 hours.
    The resulting compounds are used in industry in large quantities as antioxidants, rubbers and substances that prevent the destruction of rubbers under the action of ozone.
    Examples 1-9 (comparative examples).
    The reactions are carried out in glass autoclaves with a volume of 1 l, equipped with a diverter valve located in the bottom, a gas inlet tube, a liquid tap and a paddle stirrer (mixing using a magnetic stirrer). For the reaction, 20 g (93.2 mmol) of p-nitrosodiphenylhydroxylamine (NDGA) and 200 ml of acetone are taken. The reaction is carried out in the range from 30 to, the hydrogen pressure is 9-10 bar, the reaction time is 1 hour and the stirring speed is 1500 liters. The autoclave is first pumped out, then filled with hydrogen. Then the autoclave is half filled with the reaction medium and finally pnitrosodiphenylhydroxylamine (ndgA) and the catalyst consisting of palladium on carbon are suspended in the residue of the reaction medium and the resulting mixture is metered in through the inlet vent. The hydrogen pressure in the autoclave is then adjusted to 9-10 bar and gently heated. Depending on the amount of palladium, the reaction proceeds at a temperature of from 20 to. After cessation of heat generation, the autoclave continues to heat at 75 ° C, so that the cyt / linear reaction time is 1 h.
    In tab. 1 shows the effect of the amount of noble metal on the yield of M-isopropyl-M-phenyl-p-phenylenediamine (IFPD). In tab. 1 shows: the composition of the catalyst consisting of palladium on carbon, the amount of metal in terms of the amount of p-nitrosodiphenylhydroxylamine introduced into the reaction, as well as the yields of asymmetric H-phenyl-M-substituted p-phenylenediamine and cis forms as by-products of ketimines and non-proalkylated p-phenylenediamine derivatives.
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    The results of these comparative experiments convincingly show that when using a catalyst in an amount corresponding to 1 weight. % of palladium relative to the amount of p-nitrosodiphenylhydroxylamine introduced into the reaction, reducing reduction proceeds with a comparatively higher selectivity of the formation of the required N-isopropyl-N-phenyl-p-phenylenediamine. When using lower amounts of catalyst, the selectivity of the formation of H-isopropyl-m-phenyl-p-phenylene-. diamine drops again. When using a catalyst in an amount corresponding to 0.20 wt.% Palladium, the selectivity is significantly below 10%.
    Examples 10-21. The achieved increase in yield and selectivity due to the addition of activated carbon with a specific surface area of at least 700 and ash content less than 7.5 wt.% Can be seen from examples and comparative examples in Table. 2
    Example, 7 of table. 1 is repeated once with the addition and once without the addition of activated carbon and the conversion of the starting material and the yield of the target products are quantitatively determined depending on the duration of the reaction.
    In a census case, 60 g (280 mmol) of nitrosodiphenylhydroxylamine and 600 l of acetone in the presence of 6.0 g of a Degussa palladium-carbon catalyst with a palladium content of 1,.%, The specific surface area of coal: 1100. And ash content 0, 5 wt.% According to the method described in examples 1-9.
    In examples 17, 19 and 21, the yields of N-isopropyl-N-phenyl-p-phenylenediamine are lower than, for example, in example 15, since, due to the longer reaction time, a part of the desired product has already been further reduced to N-isopropyl-N-cyclohexyl -p-phenylenediamine.
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    1L VO f 00 L o gH tN tN tN "h tN mm Examples 22-32: Into a 1.5 l glass autoclave equipped with a paddle stirrer, thermometer, gas inlet tube, pressure gauge, liquid tap, gas vent , a bottom discharging valve, and a filtering filter filter finger, load a suspension of 20 g of p-nitrrzodiphenyl hydroxylamine and 0.8 g of palladium carbon catalyst (EIOP of Oegussa with a palladium content of 5% and 0.20% of palladium based on the amount of p-nitrosodiphenylhydroxylamine ), as well as 25 g of activated carbon (Merk Powder dried, with a specific surface area of 1050 and an ash content of less than 5 wt.% and 200. ml of methyl isobutyl ketone. After repeatedly evacuating and purging with hydrogen, the reactions are started at a hydrogen pressure of 9-10 bar. Reductive alkylation occurs at a temperature of about 40 s and after completion of the exothermic reaction during the course of which the reaction mixture is cooled, the autoclave is maintained at a stirring speed of 1500 irt, so that the total duration of the reaction is 1 hour. After completion of the reaction, the substrate using a filter press, hydrogen is separated from the hydrogenation catalyst and activated carbon-catalyst under pressure of hydrogen, and the latter are returned to the autoclave together with methyl isobutyl ketone. After that, it is reacted again for 1 hour at 75-80 ° C and a hydrogen pressure of 9-10 bar a new batch consisting of 20 g of p-nitrosodiphenylhydroxylamine, 200 g of methyl isobutyl ketone (total amount), and also of activated carbon catalyst and the corresponding cases of fresh hydrogenation catalyst. Thus, 10 cycles are carried out, during which 220 g of p-nitrosodiphenylhydroxylamine is finally subjected to reductive alkylation. The amount of hydrogenation catalyst, as well as activated carbon catalyst expressed in weight. % palladium relative to the total amount of p-nitrosodiphenylhydroxylamine introduced into the reaction, as well as the achieved yields of N- (1,3-dimethylbutyl) -N-phenyl-p-phenylenediamine (DBPPD), p-amino-diphenylamine (ADA) and ketimine are listed in the table . 3. The results indicate that after several reaction cycles, the amounts of fresh hydrogenation catalyst and activated carbon added are significantly reduced.
    ExamplesZZ-45. Examples 33-36 show both the effect of the amount of activated carbon added and the effect of the type of activated carbon (Examples 37-45) on the course of reductive alkylation.
    The reactions are carried out according to the procedure described in examples 1-9. In each case, 20 g of p-nitrozodiphenylhydroxylamine (NDGA) and 150 iJin methyl isobutyl ketone (MIBK) are introduced into the reaction. A palladium-carbon catalyst was used as the hydrogenation catalyst (Е 106R from the company Uni55a with a palladium content of 1.02% by weight).
    Synthetic activated carbons from Degusse and Merck with different values of surface and ash content, as well as various activated carbons from natural raw materials are used as activated coal.
    权利要求:
    Claims (8)
    [1]
    Examples 42-45 show that, both in cases where the specific surface area is too low, and in cases of excessively high content of activated carbon ash, the yields of N- (1,3-dimethylbutyl) -M-phenyl-p-phenylenediamine (DBPPD) are lower. Examples 46-55. Examples of the results of which are given in Table 5 show that when an activated carbon catalyst is added, the used hydrogenation catalyst largely retains its activity even in the presence of large quantities of p-fnyl-M-substituted ft-phenylenediamines (target products) so that when it is further used to achieve the initial level of activity, it is generally not necessary or required to add fresh hydrogenation catalyst in only relatively small amounts. In addition, the beneficial effect of an additional inert solvent is shown in cases where the reaction water produced is not mixed or very little mixed with the ketone used for reductive alkylation, and a second aqueous phase is formed without the addition of a cosolvent. t q-phenyl-N-tsyklogeksil-p-phenylene Claims 1. A process for preparing necim / etpichnyhN-phenyl-N-substituted p-phenylenediamines by reductive alkylation of p-nitrozodifenilgidroksilami on the aldehyde or ketone in the presence 'Wii hydrogen and palladium or platinum sulfide on carbon as catalysis. The interaction is carried out in a 1.5 l apparatus described in examples 22–32. The reaction temperature is 75-100 s, the hydrogen pressure is 9 10 bar, the reaction time is 1.5 h and the stirring speed is 10001500 irt. After each cycle is completed, a small sample is taken for analytical control of the reaction mixture and then the next batch consisting of 10 g of p-nitrosodiphenylhydroxylamine (NDHA), 50 MP cyclohexanone, is introduced to the already reacted reaction mixture under hydrogen pressure. and 50 ml of co-solvent, and depending on the number of experience, an additional amount of activated carbon catalyst or a fresh palladium-carbon catalyst. During these experiments, 10 cycles were performed, so that, in sum, reductive alkylation with cyclohexane was finally subjected to 100 g of p-nitrosodiphenylhydroxylamine (NDGD). in the presence of an inert solvent, characterized in that, in order to increase the yield and selectivity of the process, the catalyst is used in an amount corresponding to less than 1 weight. % palladium or platinum sul feed per quantity
    introduced into the reaction of p-nitrosodiphenylhydroxylamine with the addition of activated carbon with a specific surface area of not less than 700 m / g and ash content less than 7.5 weight. %
    [2]
    2, the method according to claim 1, wherein the hydrogenation catalyst is used in amounts corresponding to 0.05-0.2 weight. % palladium or platinum sulphide based on the amount of p-nitrosodiphenylhydroxy-silane entered into the reaction.
    [3]
    3, the Method according to PP. 1 and 2, characterized in that the amount of activated carbon of the catalyst is 10 -200 weight. % based on the amount of p-nitrosodiphenylhydroxylamine introduced into the reaction.
    [4]
    4, The method according to claims. 1-3, about 1 t and about the fact that the amount of aldehyde or ketone is
    2-10 eq. on each equivalent of p-nitrozaphenylhydroxylene Iin.
    [5]
    5. Method according to paragraphs. 1-4, characterized in that the reaction is carried out in the presence of an inert solvent.
    [6]
    6. A method according to claim 5, characterized in that methyl, ethyl, isopropyl, propyl or butyl alcohol, p-ethanols, isopbntanols or 4-methylpentanol-2 are used as inert solvents.
    [7]
    7. Method according to paragraphs. 1-6, characterized in that the reaction is carried out at 25-125 ° C and hydrogen pressure of 1-150 atm.
    [8]
    8. Method according to paragraphs. 1-7, about tl and 5
    h and y and so that the interaction is carried out at 40-100s and a hydrogen pressure of 7-12 atm.
    Sources of information taken into account in the examination 0 1. Patent of Great Britain No. 1295672, cl. C 2 C, pub. 08.10.72 (protoT1 -
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    同族专利:
    公开号 | 公开日
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    DE2816460A1|1979-10-25|
    DE2816460C3|1981-11-12|
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    BR7902231A|1979-12-04|
    PL117614B1|1981-08-31|
    JPS54138527A|1979-10-27|
    AT364812B|1981-11-25|
    RO76936A|1982-03-24|
    GB2018775A|1979-10-24|
    HU182842B|1984-03-28|
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    DE2816460A|DE2816460C3|1978-04-15|1978-04-15|Process for the preparation of asymmetric N-phenyl-N`-substituted p-phenylenediamines|
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