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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1076267생성일: 2026년 10월 26일

Dimethylformamide → 1,3,5-Tricarbethoxy-1,4-dihydro-2,6-dimethyl-4-(2-trifluoromethylphenyl)pyridine

https://huagongshe.com/reaction/1076267

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TetrahydrofuranHCID 8028—
반응물Sodium hydrideHCID 24758—
반응물1,4-Dihydro-2,6-dimethyl-4-(2-(trifluoromethyl)phenyl)-3,5-pyridinedicarboxylic acid diethyl esterHCID 168089—
용매AcetonitrileHCID 6342—
생성물1,3,5-Tricarbethoxy-1,4-dihydro-2,6-dimethyl-4-(2-trifluoromethylphenyl)pyridineHCID 12196458—

반응 단계

To 1.2 g. of sodium hydride (57% dispersion in mineral oil) suspended in tetrahydrofuran is added dropwise with stirring a solution of 10 g. of 3,5-dicarbethoxy-1,4-dihydro-2,6-dimethyl-4-(2-trifluoromethylphenyl)pyridine in tetrahydrofuran. The mixture is heated on a steam bath for 15 minutes, then it is cooled and enough dimethylformamide is added to dissolve the solid which has separated. To the resulting solution is added dropwise 3.04 g. of ethyl chloroformate and the reaction mixture is stirred at 25° for 15 minutes then heated on a steam bath for 12 hours. The mixture is filtered and concentrated to give an oil which is dissolved in acetonitrile. The solution is extracted with petroleum ether then concentrated to give an oil which is stirred with petroleum ether. The solid formed is filtered and the filtrate is concentrated in vacuo to give an oil which is chromatographed on an alumina "dry column" with methylene chloride as eluant to give 1,3,5-tricarbethoxy-1,4-dihydro-2,6-dimethyl-4-(2-trifluoromethylphenyl)pyridine, m.p. 56°-58°C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03956341
출처 데이터셋uspto-grants-1976_05
ORD IDord-2bd16385e24446f3a227dd5827eb0e7a
출처 메모uspto-grants-1976_05