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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1284450생성일: 2026년 10월 25일

Benzoyl chloride → (3S)-2-benzoyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

https://huagongshe.com/reaction/1284450

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl chlorideHCID 7412—
반응물Sodium HydroxideHCID 14798—
반응물boric acid, sodium saltHCID 159383—
반응물(3S)-6,7-Dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acidHCID 12926159—
용매WaterHCID 962—
생성물(3S)-2-benzoyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acidHCID 1393580982.1%

반응 단계

(3S)-6,7-Dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid [J. Org. Chem., 26, 3533 (1961)] (33.9 g) and sodium borate.10H2O (62 g) are suspended in water (500 ml). Benzoyl chloride (27.5 g) and a solution of sodium hydroxide (13 g) in water (100 ml) are added dropwise to the suspension at 0° C. under stirring. The mixture is stirred at room temperature for 4 hours. The mixture is washed with ethyl acetate, and acidified with conc. HCl, and extracted with ethyl acetate. The extract is dried and distilled to remove the solvent. The crystals are collected by filtration, washed with benzene and then recrystallized from water, whereby (3S)-2-benzoyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (41.7 g) is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04563306
출처 데이터셋uspto-grants-1986_01
ORD IDord-9bd13a5707174b40aebb5d4118cc000c
출처 메모uspto-grants-1986_01