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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358987생성일: 2026년 10월 24일

Diethyl 2-(chloromethyl)-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate → 2-(Phenylthio)methyl-3,5-dicarboethoxy-4-(m-nitrophenyl)-6-methyl-1,4-dihydropyridine

https://huagongshe.com/ko/reaction/358987

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl 2-(chloromethyl)-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylateHCID 3064723—
반응물Dimethoxyethane ethanolHCID 20074477—
반응물Sodium 2-thenoateHCID 23672340—
용매EthanolHCID 702—
생성물2-(Phenylthio)methyl-3,5-dicarboethoxy-4-(m-nitrophenyl)-6-methyl-1,4-dihydropyridineHCID 19831187—

반응 단계

A solution of 2-chloromethyl-3,5-dicarboethoxy-4-(m-nitrophenyl)-6-methyl-1, 4-dihydropyridine (5.6 g) in EtOH/DME (5/1; 20 ml) is added dropwise at +10° C. to a stirred solution of sodium thiophenate (1.8 g) in ethanol (10 ml), under N2 atmosphere. After two hours at room temperature the reaction mixture is evaporated under vacuum and the residue is partitioned between Et2O (100 ml) and water (50 ml). The organic phase is washed with a satured solution of sodium bicarbonate (2×20 ml) and water (3×20 ml), dried (Na2SO4) and evaporated to dryness. The residue is recrystallized from isopropylether to give 5.7 g of 2-(phenylthio)methyl-3,5-dicarboethoxy-4-(m-nitrophenyl)-6-methyl-1, 4-dihydropyridine, m.p. 92°-94° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04999362
출처 데이터셋uspto-grants-1991_03
ORD IDord-ccc369e802704088bd120162c649889f
출처 메모uspto-grants-1991_03