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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2277654생성일: 2026년 10월 25일

Acetic Acid → 4-Bromo-5,6,7,8-tetrahydroisoquinolin-8-OL

https://huagongshe.com/reaction/2277654

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium borohydrideHCID 4311764—
반응물4-Bromo-6,7-dihydro-8(5H)-isoquinolinoneHCID 71743380—
용매MethanolHCID 887—
생성물4-Bromo-5,6,7,8-tetrahydroisoquinolin-8-OLHCID 7174389192%

반응 조건

온도0 °C

반응 단계

4-Bromo-6,7-dihydroisoquinolin-8(5H)-one (2.135 g, 9.44 mmol) was suspended in MeOH (18.9 mL), cooled to 0° C. and treated with NaBH4 (357 mg, 9.44 mmol) in 5 portions over 30 min; then, the reaction was stirred for ¾ h at 0° C. (TLC after 30 min showed no more starting material). AcOH was then added dropwise until pH˜5-6 and the reaction mixture was evaporated. The residue was diluted with water and poured on aq. sat. NaHCO3-sol. followed by extraction with EtOAc (3×). The organic layers were washed once with aq. sat. NaHCO3-sol. and aq. 10% NaCl-sol., dried over Na2SO4 and concentrated in vacuo. The residue was re-dissolved in CH2Cl2, evaporated with n-pentane (3×) to around 20 ml each time, while the product precipitates; then, the solvent was decanted and the residue washed with n-pentane and dried in high vacuum to afford the title compound (1.98 g, 92%) as dark brown viscous oil. MS: 227 (M+, 1Br).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09133158B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-db24f0db5e9d4da5bd208f79b28e0016
출처 메모uspto-grants-2015_09