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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1781998생성일: 2026년 10월 23일

Dimethyl Sulfoxide → Benzyl 4-methylidenepiperidine-1-carboxylate

https://huagongshe.com/ko/reaction/1781998

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물Benzyl 4-oxopiperidine-1-carboxylateHCID 643496—
촉매Methyltriphenyliphosphonium bromideHCID 74505—
생성물Benzyl 4-methylidenepiperidine-1-carboxylateHCID 15519136—

반응 조건

온도60 °C

반응 단계

A sodium hydride (13.2 g) was added to an anhydrous dimethylsulfoxide (176 mL) and the mixture was heated for 2 hours at 60° C. After cooling, to a suspension of methyltriphenylphosphonium bromide (110.4 g) in dimethylsulfoxide (120 mL) was added the reaction mixture, and the mixture was stirred for 30 minutes at room temperature. To the reaction mixture was added a solution of benzyl 4-oxo-1-piperidinecarboxylate (60 g) in dimethylsulfoxide (150 mL), the mixture was stirred for 1 hour at 50° C. After cooling, to the mixture was added water (2.5 L) and the mixture was extracted with ethyl acetate (1.5 L). The organic layer was washed with a saturated aqueous solution of ammonium chloride (0.5 L) and a saturated aqueous solution of sodium chloride (0.5 L), dried and then concentrated. The obtained residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate:chloroform=9:1:1) to give the title compound (51.1 g) having the following physical data.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07498323B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-976196165fb343849eb72f934f0676e2
출처 메모uspto-grants-2009_03