돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34745생성일: 2026년 10월 24일

3-Bromoquinoline → 3-(Dimethoxyacetyl)quinoline

https://huagongshe.com/ko/reaction/34745

반응식

참여 물질

역할이름HCID투입량
반응물3-BromoquinolineHCID 21413—
반응물N-(dimethoxyacetyl)morpholineHCID 21298597—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물3-(Dimethoxyacetyl)quinolineHCID 14276934—

반응 단계

3-Bromoquinoline (3.29 ml., 0.032 mol) was dissolved in 300 ml. THF and cooled to -78°. n-Butyllithium (13.6 ml. of 2.5M in hexane, 0.034 ml.) was added slowly and the mixture stirred 15 minutes at -75° to -78°. N-(Dimethoxyacetyl)morpholine (5.98 g., 0.032 mol) in 10 ml. THF was then added and stirring continued for 1.75 hours at the same temperature. The reaction was then quenched into 300 ml. saturated NH4Cl. The aqueous layer was separated and extracted 4×100 ml. ether. The organic layers were combined, dried over MgSO4, stripped to yield title product, 7.0 g., bp 120°-123°/0.125 torr.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04762921
출처 데이터셋uspto-grants-1988_08
ORD IDord-97c01dee82af4b81ba08bf372d90172a
출처 메모uspto-grants-1988_08