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Bromo-carbonyl chloride prodn. from corresp. acid and anhydride - by reaction with bromine and phosphorus tri:bromide, and then with chlorine

机译:溴代羰基氯产品来自corresp。酸和酸酐-与溴和三溴化磷反应,然后与氯反应

摘要

Prodn. of 2-4C bromocarbonyl chlorides (I) comprises reacting the corresp. carboxylic acid and its anhydride with (a) PBr3 and Br2, then (b) with Cl2. The mole ratio acid:anhydride:PBr3:Br2:Cl2 is 1:2:1:1:15. Pref. the first stage is at -10 to 20 degrees C and subsequent chlorination at 65-95 degrees C but below the b.pt. of (I). Readily available starting materials are used (known methods start from the bromocarboxylic acid) and no special safety precautions are needed. Both steps are carried out in a single reactor without isolation of the intermediate.
机译:产品2-4C溴羰基氯(I)的反应包括使相应产物反应。羧酸及其酸酐与(a)PBr3和Br2,然后(b)与Cl2。酸:酸酐∶PBr 3 ∶Br 2 ∶Cl 2的摩尔比为1∶2∶1∶1∶15。首选第一阶段是在-10至20摄氏度,随后在65-95摄氏度但低于沸点的条件下进行氯化。 (I)。使用现成的原料(已知方法从溴代羧酸开始),并且不需要特殊的安全预防措施。这两个步骤均在单个反应器中进行,无需分离中间体。

著录项

  • 公开/公告号DE2919198A1

    专利类型

  • 公开/公告日1980-11-20

    原文格式PDF

  • 申请/专利权人 CHEMISCHE FABRIK KALK GMBH;

    申请/专利号DE19792919198

  • 发明设计人 KOENIGSTEINOTTODR.;JENKNERHERBERTDR.;

    申请日1979-05-12

  • 分类号C07C51/58;C07C53/50;C07C53/48;

  • 国家 DE

  • 入库时间 2022-08-22 15:16:28

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