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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358988생성일: 2026년 10월 25일

Monoperoxyphthalic acid → 2-(Phenylsulfinyl)methyl-3,5-dicarboethoxy-4-(m-nitrophenyl)-6-methyl-1,4-dihydropyridine

https://huagongshe.com/reaction/358988

반응식

참여 물질

역할이름HCID투입량
반응물Monoperoxyphthalic acidHCID 75329—
반응물Sodium BicarbonateHCID 516892—
반응물2-(Phenylthio)methyl-3,5-dicarboethoxy-4-(m-nitrophenyl)-6-methyl-1,4-dihydropyridineHCID 19831187—
용매Ethyl AcetateHCID 8857—
생성물2-(Phenylsulfinyl)methyl-3,5-dicarboethoxy-4-(m-nitrophenyl)-6-methyl-1,4-dihydropyridineHCID 19831202—

반응 단계

A solution of monoperphtalic acid in AcOEt (0.37 M solution; 20 ml) is added at 0° C. to a mixture of 2-(phenylthio)methyl-3, 5-dicarboethoxy-4-(m-nitrophenyl)-6-methyl-1,4-dihydropyridine (3.5 g) and NaHCO3 (3 g) in AcOEt (20 ml). After 30 minutes the mixture is filtered and the eluate is washed with 1N solution of sodium thiosulfate (2 ×10 ml), with a saturated solution of NaHCO3 (2×20 ml) and then with water (3×10 ml). The organic layer is dried on Na2SO4 and evaporated to dryness; the residue is purified by chromatography on SiO2 (hexane/AcOEt 85/15, as eluent) to give 3.5 g of 2-(phenylsulfinyl)methyl-3,5-dicarboethoxy-4-(m-nitrophenyl) -6-methyl-1,4-dihydropyridine, m.p. 160°-162° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04999362
출처 데이터셋uspto-grants-1991_03
ORD IDord-ce929d93de2e4375bbe94fc1fd258f7b
출처 메모uspto-grants-1991_03