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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 879992생성일: 2026년 10월 25일

Triphenylphosphine → 1-(3-Bromo-4-{[(4-chloro-2-pyridinyl)methyl]oxy}phenyl)ethanone

https://huagongshe.com/reaction/879992

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물1-(3-Bromo-4-hydroxyphenyl)ethanoneHCID 608094—
반응물(4-Chloropyridin-2-yl)methanolHCID 2763167—
반응물Diethyl azodicarboxylateHCID 5462977—
용매TetrahydrofuranHCID 8028—
생성물1-(3-Bromo-4-{[(4-chloro-2-pyridinyl)methyl]oxy}phenyl)ethanoneHCID 68201960—

반응 단계

To a stirred solution of (4-chloro-2-pyridinyl)methanol (Commercial eg Aldrich) (0.2 g) in THF (5 ml) were added 1-(3-bromo-4-hydroxyphenyl)ethanone (0.3 g) and triphenylphosphine (0.547 g). This was stirred for 10 min before cooling and adding slowly DEAD (0.363 g). This was stirred for 16 h. The reaction mixture was partitioned between water and ethyl acetate. The aqueous was reextracted with ethyl acetate and the combined organics were washed with brine, dried over sodium sulfate and concentrated in vacuo. This was purified through silica eluting with 0-35% ethyl acetate in hexane to give the title compound, 0.30 g

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08993560B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-0afcd3a3bfe04c7e9f8e70e335a340dd
출처 메모uspto-grants-2015_03