首页> 外文期刊>Monatshefte für Chemie / Chemical Monthly >Efficient synthesis of functionalized 2,5-dihydrofurans and 1,5-dihydro-2H-pyrrol-2-ones by reaction of isocyanides with activated acetylenes in the presence of hexachloroacetone
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Efficient synthesis of functionalized 2,5-dihydrofurans and 1,5-dihydro-2H-pyrrol-2-ones by reaction of isocyanides with activated acetylenes in the presence of hexachloroacetone

机译:在六氯丙酮存在下,通过异氰酸酯与活化乙炔的反应,高效合成官能化的2,5-二氢呋喃和1,5-二氢-2H-吡咯-2-酮

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摘要

Isocyanides react smoothly with dimethyl acetylenedicarboxylate in the presence of hexachloroacetone to produce dimethyl 5-[alkyl(aryl)imino]-2,2-bis(trichloromethyl)-2,5-dihydro-furan-3,4-dicarboxylates in high yields. When the reaction was performed with dibenzoylacetylene, 3-benzoyl-1-alkyl-4-chloro-5-hydroxy-5-phenyl-1,5-dihydro-2H-pyrrol-2-ones were obtained.
机译:异氰化物在六氯丙酮的存在下与乙炔二甲酸二甲酯平稳反应,以高收率产生5- [烷基(芳基)亚氨基] -2,2-双(三氯甲基)-2,5-二氢呋喃-3,4-二羧酸二甲酯。用二苯甲酰基乙炔进行反应时,得到3-苯甲酰基-1-烷基-4-氯-5-羟基-5-苯基-1,5-二氢-2H-吡咯-2-酮。

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