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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35240생성일: 2026년 10월 24일

Triethylamine → N-(4-acetoxyphenylacetyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-methylisoquinoline

https://huagongshe.com/ko/reaction/35240

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물6,7-Dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinolineHCID 10302—
반응물Benzeneacetyl chloride, 4-(acetyloxy)-HCID 182488—
용매ChloroformHCID 6212—
생성물N-(4-acetoxyphenylacetyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-methylisoquinolineHCID 2129581090.1%

반응 단계

To a stirred solution of 1,2,3,4-tetrahydro-6,7-dimethoxy-1-methylisoquinoline (20.0 g, 0.097 m) and triethylamine (9.8 ml, 0.097 m) in chloroform (200 ml) under nitrogen was added dropwise a solution of 4-acetoxyphenylacetyl chloride (20.3 g, 0.097 m) in 50 ml chloroform and the mixture stirred at ambient temperature for 16 hours. The mixture was washed with 10% HCl (3×200 ml), water (200 ml), saturated sodium carbonate (3×150 ml) and water (200 ml) and the chloroform layer dried over MgSO4. Evaporation of the solvent afforded 33.0 g of N-(4-acetoxyphenylacetyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-methylisoquinoline as a pale yellow oil (89% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04766131
출처 데이터셋uspto-grants-1988_08
ORD IDord-03615a9232a543cdbced5ab10d137e44
출처 메모uspto-grants-1988_08