돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 920896생성일: 2026년 10월 24일

Phosphonium, (bromomethyl)triphenyl-, bromide (1:1) → (Z)-2-(2-bromovinyl)-6-fluoroquinoline

https://huagongshe.com/ko/reaction/920896

반응식

참여 물질

역할이름HCID투입량
반응물Phosphonium, (bromomethyl)triphenyl-, bromide (1:1)HCID 2733422—
반응물6-Fluoroquinoline-2-carbaldehydeHCID 3159605—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물(Z)-2-(2-bromovinyl)-6-fluoroquinolineHCID 8668311365.4%

반응 단계

To as suspension of (bromomethyl)triphenylphosphonium bromide (14.94 g, 34.3 mmol) in 100 mL of THF was added potassium tert-butoxide (3.84 g, 34.3 mmol) portionwise under Ar. Then the reaction mixture was stirred for 1 h at this temperature. 6-Fluoroquinoline-2-carbaldehyde (5 g, 28.5 mmol) in 40 mL of THF was added. The resulting reaction mixture was stirred for 5 h at −75° C. and allowed to warm up overnight. The reaction mixture was diluted with petrol ether and the solid was sucked off. The mother liquid was concentrated, diisopropyl ether was added and the formed precipitate was sucked off. The mother liquid was purified by column chromatography (cyclohexane/EA) to give 4.7 g (65.3%) of the title compound as brown solid. LC-MS: m/e 254.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09273068B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-20c5ec6bafca4fb0a9ce6892d8c2c734
출처 메모uspto-grants-2016_03