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PREPARATION OF 2,5-HEXANEDIONE

机译:2,5-己二酮的制备

摘要

PURPOSE:To obtain the titled compound useful as an intermediate for a perfume, an insecticide or a medicine, readily in a short stage, by condensing a readily available acetoacetic ester with a monohalogenoacetone, and saponifying and decarboxylating the condensate. CONSTITUTION:An acetoacetic ester expressed by formula I (R is alkyl) is reacted with a monohalogenoacetone expressed by formula II (X is Cl, Br or I) in the presence of a base, e.g. an alkali metallic hydroxide or an alkali metallic alkoxide, in a polar solvent, at -10-25 deg.C, to prepare 2-acetyllevulinic acid. When a polar nonaqueous solvent is used as the reaction solvent, the solvent is eliminated, and the 2-acetyllevulinic acid is saponified in the presence of a mineral acid, alkaline hydroxide, etc., and subsequently decarboxylated, to give the aimed compound. A mineral or organic acid which enables the simultaneous decarboxylation, may be preferably used for the saponification. When water is used as the reaction solvent, the saponification occurs at the same time with the acetonylation.
机译:目的:通过将容易获得的乙酰乙酸酯与单卤代丙酮缩合,然后将缩合物皂化和脱羧,以在短时间内容易地获得用作香料,杀虫剂或药物中间体的标题化合物。组成:在碱的存在下,将式I(R为烷基)表示的乙酰乙酸酯与式II(X为Cl,Br或I)表示的单卤代丙酮反应。在极性溶剂中于-10-25℃下用碱金属氢氧化物或碱金属醇盐制备2-乙酰基乙酰丙酸。当使用极性非水溶剂作为反应溶剂时,除去溶剂,并且在无机酸,碱性氢氧化物等的存在下将2-乙酰基乙酰丙酸皂化,然后脱羧,得到目标化合物。能够同时脱羧的无机酸或有机酸可优选用于皂化。当使用水作为反应溶剂时,皂化与乙酰化同时发生。

著录项

  • 公开/公告号JPS56169639A

    专利类型

  • 公开/公告日1981-12-26

    原文格式PDF

  • 申请/专利权人 ASAHI CHEMICAL IND;

    申请/专利号JP19800074688

  • 申请日1980-06-03

  • 分类号C07C43/03;C07C41/00;C07C45/00;C07C45/61;C07C49/12;C07C67/00;

  • 国家 JP

  • 入库时间 2022-08-22 14:15:30

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