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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2142생성일: 2026년 10월 24일

Triethylamine → N-(3,4-Dimethoxybenzenesulphonyl)-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/ko/reaction/2142

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1,2,3,4-TetrahydroquinolineHCID 69460—
반응물3,4-Dimethoxybenzenesulfonyl chlorideHCID 2734183—
용매DichloromethaneHCID 6344—
생성물N-(3,4-Dimethoxybenzenesulphonyl)-1,2,3,4-tetrahydroquinolineHCID 667562—

반응 단계

1,2,3,4-Tetrahydroquinoline (0.29 ml) was added to a suspension of 3,4-dimethoxybenzene sulphonyl chloride (0.50 g) in dichloromethane (15 ml) at room temperature. Triethylamine (0.44 ml) was added and the resulting mixture stirred for 24 hours at room temperature. The reaction mixture was then diluted with dichloromethane (20 ml) and washed successively with saturated aqueous sodium hydrogen carbonate solution (10 ml), 2N hydrochloric acid (10 ml) and saturated aqueous sodium chloride solution (10 ml). Drying over magnesium sulphate and concentration in vacuo provided a yellow oil. Purification by column chromatography eluting with 30% ethyl acetate in hexane provided the title compound as a colourless oil (0.60 g) which solidified on standing.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728712
출처 데이터셋uspto-grants-1998_03
ORD IDord-80b4d3c6a338477cbce6e4a97e49acd8
출처 메모uspto-grants-1998_03