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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26479생성일: 2026년 10월 26일

Phenethyl bromide → N-Phenethyl-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline

https://huagongshe.com/reaction/26479

반응식

참여 물질

역할이름HCID투입량
반응물Phenethyl bromideHCID 7666—
반응물PentaneHCID 8003—
반응물Sodium hydrideHCID 24758—
반응물4a-(m-Methoxyphenyl)-1,3-diketo-trans-decahydroisoquinolineHCID 86736478—
용매DimethylformamideHCID 6228—
생성물N-Phenethyl-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinolineHCID 13282015—

반응 단계

A solution of 10.0 g (37 mmoles) of 4a-(m-methoxyphenyl)-1,3-diketo-trans-decahydroisoquinoline in 250 ml of anhydrous dimethylformamide was added with stirring to a suspension of 2.8 g (55.5 mmoles) of 50% sodium hydride in mineral oil (washed with pentane) in 125 ml of anhydrous dimethylformamide heated at 50° under nitrogen. The mixture was heated at 90° for 2 hours, then cooled to 40°, at which time a solution of 14.0 g (74 mmoles) of phenethyl bromide in 20 ml of anhydrous dimethylformamide was added and the reaction mixture heated at 90° overnight. The cooled solution was poured into ice-water and extracted with ether. Evaporation of the ether gave an oil which was purified by column chromatography (Silicar CC-7, eluting with acetone-benzene). The major fraction was identified as N-phenethyl-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04150135
출처 데이터셋uspto-grants-1979_04
ORD IDord-39d377ee3df3459fbf811c3daf211de4
출처 메모uspto-grants-1979_04