• 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:
    A process for preparing substituted phthalic anhydrides, e.g. 4-methylphthalic anhydride, in which the Diels-Alder addition product of a conjugated diene, e.g. isoprene, and maleic anhydride is reacted with bromine in the presence of an acid acceptor. The acid acceptor can be present in catalytic amounts. Typical acid acceptors include dimethylformamide and pyridine.
    公开号:SU1373320A3
    申请号:SU853882455
    申请日:1985-04-11
    公开日:1988-02-07
    发明作者:Е.Телшоу Джеффри
    申请人:Стауффер Кемикал Компани (Фирма)；
    IPC主号:
    专利说明:

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    The invention relates to an improved process for the preparation of D-methylphthalic anhydride, which can be used for the production of herbicides.
    The aim of the invention is to increase the yield of the target product by changing the conditions of the process.
    The Diels-Alder addition products according to p1 of the proposed method are obtained by reacting maleic acid with a conjugated diene. The conjugated diene may include butadiene, 2,3-dimethyl butadiene, other substituted butadiene, and preferably isoprene.
    The addition product is obtained by reacting maleic anhydride with a co-conjugated diene under a nitrogen atmosphere. Maleic anhydride is heated to melt, then conjugated diene is added slowly under the surface of the melt. When the addition of the diene is complete, the reagents are heated to a reaction temperature of 55 to 120 ° C, with preferred temperatures of Vep-x-Noh of 00-20 ° C. Reagents are held in the temperature range of the reaction until the end of the latter, usually about 1 The reaction may be exometric, therefore external cooling is required to maintain the reactants within the temperature range of the reaction. After completion of the reaction, upon formation of an adduct, an excess of diene is removed from the reaction zone by vacuum at pressures that reduce the sublimation of the adduct.
    The reaction used to obtain the adduct may proceed in the presence or absence of a solvent. However, when the acid acceptor is added only in catalytic amounts, preferably no solvent is present. Dimethylformamide (DMF) can be a suitable solvent. When DMF is used, a solution of the adduct in DMF is obtained and no solid phase is formed during the reaction. The bromination step is carried out directly with a solution of DMF and the adduct after removal of excess diene from the reaction zone. AT
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    In this case, DMF behaves as a solvent and as an acid acceptor.
    The Diels-Alder addition reaction stoichiometry typically includes 1 mole of maleic anhydride, which reacts with 1 mole of conjugated diene to make 1 mole of the addition product, therefore, from an economic point of view, it is desirable to introduce into the interaction equimolar amounts of reagents. However, a molar excess of diene is used.
    When the Diels-Alder reaction addition product is used as a starting material and the acidic acceptor is present in an amount exceeding the catalytic amount, then the addition product is converted into solution by means of a solvent and an acidic acceptor is added to this solution. Chlorobenzene and DMF can serve as solvents. When DMF is used as a solvent, substantial amounts are used, so that DMF can also participate as an acid acceptor in the reaction.
    Bromine is then slowly added to the reactor. After that, an adduct of hydrogen bromide / acid acceptor begins to form, which may or may not precipitate out of solution. Addition of bromine can give exometomaticity from weak to medium. During the addition of bromine, the temperature in the reaction zone is maintained between 35 and 150 ° C. When a solvent is used in the reaction, it is preferred that the temperature be within the range from to the boiling point of the solvent. When the addition of bromine is complete, the temperature in the reaction zone is slowly raised to-180 ° C to ensure that the process is complete.
    Upon completion of the reaction, an inaccurate solution remains inside the reactor. The crude solution is then cooled to O - 60 ° C and then water is added. Two separate layers are formed - aqueous and organic, which can be separated. When using DMF as a solvent and an acid acceptor, chloroform is used to extract the substituted phthalic anhydride, which is added before water is added, and the aqueous layer can be washed
    chloroform after separation of the layers. Chlorobenzene can also be used as an extracting and washing agent. The organic layers are then combined, concentrated and distilled to form the desired final product, the substituted phthalic anhydride.
    When a Diels-Alder reaction addition product is used as the starting material and the acid acceptor is used in a catalytic amount, according to the inventive method, the addition product is heated in a reactor having a nitrogen atmosphere to melt it. An acidic acceptor catalyst is first added to the melt, then the temperature is raised to -120 ° C. Bromine is then slowly added under the surface of the melt. Thereafter, the hydrogen bromide begins to slowly release, and then the emission increases to a fairly constant rate. The addition of bromine can be adjusted to such a rate that none of the characteristic colors of bromine can develop in connection with the liberated hydrogen bromide, with the addition of bromine, the exothermicity is regulated from weak to medium. During the addition of bromine, the temperature in the reaction zone is maintained / -lOO-lSO C (preferably between 1 and 35-145 ° C). After the addition of bromine is complete, the temperature inside the reaction zone is slowly raised to-180 ° C to ensure that the reaction is complete. This is manifested in the termination of the release of hydrogen bromide. A bubbler containing mineral oil in the output line is used to control the release of hydrogen bromide.
    Upon completion of the reaction, a crude melt remains in the reactor, which is distilled, after a water treatment, which gives high purity 4-methylphthalic (4-MFA) anhydride.
    Example 1. In a three-liter flask with a capacity of 1 l, equipped with a dropping funnel, a mechanical blender, a storage thermometer and a condenser, 98.1 g (1.0 mmol) of maleic anhydride are placed. The flask is heated in an oil bath until the acid anhydride melts. Isoprene (69.5 g, 1.02 mol) is then added dropwise below the surface level.
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    molten maleic anhydride, using an additional tube of fluorocarbon polymer Teflon polymer attached to a dropping funnel, at a rate that minimizes distillation. The temperature of the interacting substances in the flask is controlled with periodic cooling and maintained in the range of 55-100 C.
    After completion of the addition of isoprene, the reaction flask is heated to and maintained at this temperature for 60 minutes to ensure complete completion of the reaction. Excess isoprene is then removed from the reactor at 100 mm / 90 ° C for 20 minutes.
    Melted 4-methyl-I, 2,3,6-tetrahydro-phthalic anhydride (4-MTFA, mp 58-63 ° C) yellowish remains in the reaction flask.
    Example2. In a three-neck flask, a solution is prepared from 16.6 g (0.10 mol) of 4-MTFA in 60 ml of chlorobenzene and 32.7 ml (32, g, 0.404 mol) of pyridine. Bromine (10.3 ml, 32.1 g, 0.202 mol) is added dropwise to this solution.
    When bromine is added, the temperature of the interacting compounds increases and reaches 30-42 ° C. This temperature range is maintained until the addition of bromine is completed, then the interacting compounds are heated to and maintained at this temperature for 30 minutes.
    The temperature of the interacting compounds is reduced to 25 ° C and 100 ml of water is added to the flask. The two phases that form are separated and the aqueous phase is further extracted with two portions in 25 ml of chlorobenzene. The combined organic fractions are concentrated under high vacuum to obtain 14.1 g (yield 87%) of a yellow solid. Analysis by gel chromatography and NMR shows that it is pure 4-MFA.
    Example 3: This is a generic procedure.
    Molten 4-MTFA (166.1 g, 1.0 mol) was prepared in a three-necked flask without solvent, as in Example I. Dimethylformamide (5.0 g, 0.068 mol) was added to the flask. The contents of the flask are then heated to 1–20 ° C and mechanically mixed, simultaneously
    adding bromine (103.5 ml, 322.8 g, 2.02 mol) dropwise below the melt level. The temperature in the reactor rises to 140 ° C and is maintained in the range of 135-145 ° C for the entire period of addition of bromine (2.5-3.5 hours) by thermostatic control in an oil bath at a temperature of 140-145 ° C. Bromist hydrogen is released a few minutes after the start of the addition of bromine, it is neutralized in a lovuvzh containing sodium hydroxide solution. The rate of addition of bromine is set in such a way that the color of bromine in the hydrogen bromide liberated is not observed
    After the end of the addition of bromine, the temperature of the dark brown melt is maintained at 140 ° C for 15 minutes and then slowly raised to 180 ° C in order to complete the release of hydrogen bromide. After maintaining the temperature at 180 ° C for 1 hour, the remaining crude brown melt is distilled from the flask using a 3 Vigreaux column and a short, non-cooled condenser. A pale yellow distillate (bp 153-157 ° C) is collected under a pressure of 7 mm Hg. After cooling, solid 4 methylf1 alyl anhydride remains. L weighing 24-130 g (76-80%), so pl. 78-89 with an analysis using high pressure liquid chromatography shows a purity of 95%.
    EXAMPLE 4 Molten D-MTPL (166.1 g, 1.0 mol) was prepared as in Example 1. Pyridine (8.5 ml, 8.3 g, O, 105) was added to the flask. mole).
    While stirring with a mechanical stirrer, the temperature of the contents of the flask is maintained at 105-120 ° C while simultaneously adding bromine (103.5 ml, 322.8 g, 2.02 mol) dropwise under the surface of the melt for 3.5 hours.
    Hydro-bromide is continuously released. After the addition was complete, the temperature of the reaction flask was maintained for 2 hours. Analysis by gel chromatography shows that the reaction was incomplete, therefore another 10 ml of bromine is added at II ~ 120 ° C for 40 minutes. The dark brown melt is then heated to 150-155 ° C for 4 h to complete the release of hydrogen bromide.
    With melt, the melt is distilled under vacuum, as in Example 4. After a small amount, the main fraction is collected at b.p. 129-131 ° C 1,5 mmrts White solid 4-MFA, obtained by cooling, weighs PO, / g (yield 62%), purity, as shown by analysis using liquid chromatography under high pressure, 90%.
    权利要求:
    Claims (2)
    [1]
    1. A method of producing 4-methylphthalic anhydride by reacting maleic anhydride with isoprene, followed by reacting the resulting addition product of the Diels-Alder reaction with bromine and isolating the target product, characterized in that, in order to increase the yield of the target product, the reaction with bromine is carried out in the presence of pyr1 or dimethylformamide at a molar ratio of anhydride: bromine: pyridine or dimethylformamide 1: (2.02-2.22) :( 0.068-0.105) at 105-180 ° С or in the presence of pyridine at a molar ratio of anhydride: bromine : pyridine 1: 2,02: 4,04 in the environment of chlorobenzene at 30-70 ° C.
    [2]
    2. The method according to claim 1, wherein the desired product is recovered directly by distillation.
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    同族专利:
    公开号 | 公开日
    DE3576338D1|1990-04-12|
    MX156959A|1988-10-17|
    BR8501518A|1985-11-26|
    HU195202B|1988-04-28|
    AU4123085A|1985-10-24|
    CA1226870A|1987-09-15|
    ES8603453A1|1985-12-16|
    HUT37775A|1986-02-28|
    IE58213B1|1993-08-11|
    AU570551B2|1988-03-17|
    IL74529D0|1985-06-30|
    EP0159637B1|1990-03-07|
    EP0159637A1|1985-10-30|
    ES542305A0|1985-12-16|
    IL74529A|1989-03-31|
    IE850951L|1985-10-16|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US2264429A|1941-12-02|Process fob preparing substituted |
    US2391226A|1943-02-25|1945-12-18|Wingfoot Corp|Method of preparing a cyclic dicarboxylic acid anhydride|
    JPS5822460B2|1977-04-06|1983-05-09|Mitsui Toatsu Chemicals|JPH0276871A|1987-07-10|1990-03-16|New Japan Chem Co Ltd|Production of methyltetrahydrophthalic anhydride|
    US4785120A|1987-07-27|1988-11-15|Stauffer Chemical Company|Process for preparing substituted phthalic anhydrides|
    FR2674248B1|1991-03-19|1993-06-11|Elf Aquitaine|PROCESS FOR CHEMICAL MODIFICATION OF PROTEINS.|
    CN102702149A|2012-07-09|2012-10-03|张家港市贝利化学品有限公司|Method for preparing 4-methyl benzene anhydride|
    CN105001187A|2015-06-29|2015-10-28|贝利化学（张家港）有限公司|Vapor phase method for preparing 4-methylphthalic anhydride|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    US06/600,247|US4560773A|1984-04-16|1984-04-16|Process for preparing substituted phthalic anhydrides|
    US06/600,248|US4559405A|1984-04-16|1984-04-16|Process for preparing substituted phthalic anhydrides|
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