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首页> 外文期刊>The Korean journal of chemical engineering >O-alkylation of disodium salt of diethyl 3,4-dihydroxythiophene-2,5-dicarboxylate with 1,2-dichloroethane catalyzed by ionic type phase transfer catalyst and potassium iodide
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O-alkylation of disodium salt of diethyl 3,4-dihydroxythiophene-2,5-dicarboxylate with 1,2-dichloroethane catalyzed by ionic type phase transfer catalyst and potassium iodide

机译:离子型相转移催化剂和碘化钾催化1,2-二氯乙烷催化3,4-二羟基噻吩-2,5-二羧酸二乙酯二钠盐的O-烷基化

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摘要

Diethyl 3,4-ethylenedioxythiophene-2,5-dicarboxylate was efficiently synthesized via the O-alkylation of disodium salt of diethyl 3,4-dihydroxythiophene-2,5-dicarboxylate with 1,2-dichloroethane over ionic type phase transfer catalysts, such as tetrabutyl ammonium bromide and benzyltriethyl ammonium chloride. The ionic type phase transfer catalysts showed higher catalytic activities than the nonionic type phase transfer catalysts, such as triethylamine, pyridine, 18-crown-6, and polyethylene glycol 400/600, in the O-alkylation reaction. The conversion of the disodium salt of more than 97% and the selectivity of diethyl 3,4-ethylenedioxythiophene-2,5-dicarboxylate of more than 98% were achieved when the O-alkylation reaction was synergistically catalyzed by tetrabutyl ammonium bromide and potassium iodide.
机译:在离子型相转移催化剂上,通过1,2-二氯乙烷对3,4-二羟基噻吩-2,5-二羧酸二乙酯的二钠盐进行1,2-二氯乙烷的O-烷基化反应,可以有效地合成3,4-乙烯二氧噻吩-2,5-二羧酸二乙酯。为四丁基溴化铵和苄基三乙基氯化铵。在O-烷基化反应中,离子型相转移催化剂显示出比非离子型相转移催化剂更高的催化活性,例如三乙胺,吡啶,18-crown-6和聚乙二醇400/600。当四丁基溴化铵和碘化钾协同催化O-烷基化反应时,二钠盐的转化率超过97%,3,4-亚乙基二氧噻吩-2,5-二羧酸二乙酯的选择性达到98%以上。

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