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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 398325생성일: 2026년 10월 23일

1,2,3,4-Tetrahydroisoquinoline → 3,4-Dihydroisoquinoline

https://huagongshe.com/ko/reaction/398325

반응식

참여 물질

역할이름HCID투입량
반응물1,2,3,4-TetrahydroisoquinolineHCID 7046—
반응물Sodium HydroxideHCID 14798—
반응물N-bromobutanimideHCID 67184—
용매DichloromethaneHCID 6344—
생성물3,4-DihydroisoquinolineHCID 76705—

반응 단계

9.4 ml of 1,2,3,4-tetrahydroisoquinoline are dissolved in 200 ml of DCM and 14.7 g of NBS are gradually added. The mixture is left stirring at RT, cooling slightly in order to maintain a temperature of less than 40° C. for 30 minutes, after which 50 ml of 10N NaOH are added and the mixture is left stirring for 1 hour at RT. The organic phase is separated out after settling of the phases has taken place and is washed with 100 ml of water and then twice with 100 ml of 4N HCl. The aqueous phases are washed with DCM and then brought to pH=9 by addition of concentrated NH4OH. This mixture is extracted with DCM, dried over Na2SO4 and evaporated to dryness. The oil obtained is distilled off. 7.16 g of the expected compound are obtained, b.p.=50-54° C. at 0.05 mbar.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610882B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-17009ae711264a15b780897882dd2b0a
출처 메모uspto-grants-2003_08