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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48212생성일: 2026년 10월 24일

5-Bromo-8-nitroisoquinoline → 5-bromo-8-nitro-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/ko/reaction/48212

반응식

참여 물질

역할이름HCID투입량
반응물5-Bromo-8-nitroisoquinolineHCID 816983—
반응물Sodium cyanoborohydrideHCID 5003444—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물5-bromo-8-nitro-1,2,3,4-tetrahydroisoquinolineHCID 10038065—

반응 단계

Alternatively, a solution of 5-bromo-8-nitroisoquinoline (1.0 g) in glacial acetic acid (30 mL) was cooled to 0° C. and, before freezing, was treated with sodium cyanoborohydride (1.10 g). The reaction mixture was warmed slowly to room temperature under nitrogen. The reaction mixture was diluted with water and basified. Organic layer extracts were chromatographed on silica gel as before.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06703391B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-92c435d16a5e4d599305b982937720f7
출처 메모uspto-grants-2004_03