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Liquid phase preparation of 2-H-2-oxazolines and 2-substituted-2- oxazolines

机译:2-H-2-恶唑啉和2-取代-2-恶唑啉的液相制备

摘要

2-H-2-Oxazolines are prepared by contacting in liquid phase a N-(&bgr; -hydroxyalkyl)formamide with a small but catalytic amount of an inorganic zinc salt at elevated temperatures. Similarly, 2-substituted-2- oxazolines are prepared by contacting N-(2-hydroxyalkyl)carboxamides with a small but catalytic amount of an inorganic zinc salt. As an example, 2- H-2- oxazoline was prepared in approximately 72 percent yield by warming a mixture of N-(&bgr;-hydroxyethyl)formamide with a catalytic amount of zinc chloride at a temperature of from 180° C. to 185° C. /50 mm Hg for 2.2 hours. In this reaction, the desired oxazoline product was recovered as a codistillate with water during the course of the reaction.
机译:2-H-2-恶唑啉是通过在升高的温度下使液相的N-(α-羟烷基)甲酰胺与少量但催化量的无机锌盐接触而制备的。类似地,通过使N-(2-羟烷基)羧酰胺与少量但催化量的无机锌盐接触来制备2-取代的2-恶唑啉。例如,通过在180℃至185℃的温度下加热N-(b-羟乙基)甲酰胺与催化量的氯化锌的混合物以约72%的产率制备2-H-2-恶唑啉。 / 50毫米汞柱持续2.2小时。在该反应中,在反应过程中将所需的恶唑啉产物与水作为共馏物回收。

著录项

  • 公开/公告号US4443611A

    专利类型

  • 公开/公告日1984-04-17

    原文格式PDF

  • 申请/专利权人 THE DOW CHEMICAL COMPANY;

    申请/专利号US19820415077

  • 发明设计人 MARK E. KAISER;

    申请日1982-09-07

  • 分类号C07D207/20;

  • 国家 US

  • 入库时间 2022-08-22 08:39:01

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