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苯氧菌酯的合成研究
引用本文:刘卫东,徐道庄,杜升华,吴光群.苯氧菌酯的合成研究[J].精细化工中间体,2003,33(4):10-11.
作者姓名:刘卫东  徐道庄  杜升华  吴光群
作者单位:湖南化工研究院,湖南,长沙,410007
摘    要:以苯酞和邻甲酚为起始原料 ,生成物经酰氯化、酰氰化、水解反应得苯基草酸甲酯衍生物 ,再与甲氧基氨盐酸反应得Z/E构型混合物。该混合物经转位反应得苯氧菌酯。反应总收率为 5 7 2 % (以苯酞计 ) ,产品纯度为 95 %。该工艺流程简单 ,易于工业化生产

关 键 词:苯氧菌酯  邻甲酚  苯酞  合成
文章编号:1009-9212(2003)04-0010-02
修稿时间:2003年5月8日

The Synthesis Study on Kresoxim-methyl
LIU Wei,dong etc..The Synthesis Study on Kresoxim-methyl[J].Fine Chemical Intermediates,2003,33(4):10-11.
Authors:LIU Wei  dong etc
Abstract:Kresoxim methyl was prepared by reacting the intermediate, methyl 2 (2 methylphenoxymethyl) phenylglyoxylate, with O-methylhydroxylamine hydrochloride. The resulting E/Z isomer mixture was treated with hydrochloride for substantial rearrangement of the Z to the E isomer. The intermediate was synthesized by using O cresol, phthalide, thionyl chloride, and sodium cyanide as raw materials. The total yield of the five steps reaches 57.2% (according to phthalide), and the process is convinient and suitable for the industrial manufacture.
Keywords:Kresoxim-methyl  O  cresol  phthalide  synthesis
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