首页> 外国专利> PREPARATION OF 4-BROMOMETHYL-5-METHYL-1,3-DIOXOL-2-ONE

PREPARATION OF 4-BROMOMETHYL-5-METHYL-1,3-DIOXOL-2-ONE

机译:4-溴甲基-5-甲基-1,3-二氧戊-2-酮的制备

摘要

PURPOSE:To improve the yield of the titled compound useful as an intermediate of pharmaceuticals in the bromination of 4,5-dimethyl-1,3-dioxol-2-one with molecular bromine under specific condition, by heat-treating the reaction mixture under specific condition after the completion of the reaction. CONSTITUTION:4,5-Dimethyl-1,3-dioxol-2-one of formulaIis brominated economically by reacting with economically available molecular bromine in an inert solvent at 10-90 deg.C, preferably 30-85 deg.C. The obtained reaction mixture is, if necessary after the removal of the inert slovent therefrom, heat-treated at 95- 160 deg.C, preferably at 100-150 deg.C for =1hr, preferably =1.5hr to convert a part of the dibrominated compound by-produced in the bromination reaction to the objective compound. The 4-bromomethyl-5-methyl-1,3-dioxol-2-one of formula II can be prepared in high yield by this process.
机译:目的:通过在特定条件下对反应混合物进行热处理,以提高标题化合物的产率,该标题化合物用于在特定条件下用分子溴溴化4,5-二甲基-1,3-二氧杂-2-酮的药物中间体反应完成后的特定条件。组成:式I的4,5-二甲基-1,3-二氧杂-2-酮可通过与经济上可得的分子溴在惰性溶剂中于10-90℃,优选30-85℃反应经济地溴化。如果需要,将得到的反应混合物从其中除去惰性溶剂之后,在95-160℃,优选在100-150℃下热处理≥= 1小时,优选≥= 1.5小时以转化一部分。在溴化反应中副产物二溴化化合物的生成量为目标化合物。通过该方法可以高收率地制备式II的4-溴甲基-5-甲基-1,3-二氧杂-2-酮。

著录项

  • 公开/公告号JPS58152879A

    专利类型

  • 公开/公告日1983-09-10

    原文格式PDF

  • 申请/专利权人 MITSUBISHI KASEI KOGYO KK;

    申请/专利号JP19820034808

  • 发明设计人 TAKEDA YOSHIYUKI;YAMADA KENICHI;

    申请日1982-03-05

  • 分类号C07D317/40;

  • 国家 JP

  • 入库时间 2022-08-22 11:35:30

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