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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 865864생성일: 2026년 10월 24일

4-Bromodiphenyl Ether → 1-(4-Phenoxyphenyl)prop-2-en-1-ol

https://huagongshe.com/ko/reaction/865864

반응식

참여 물질

역할이름HCID투입량
반응물4-Bromodiphenyl EtherHCID 7565—
반응물AcroleinHCID 7847—
반응물HCID 178418306HCID 178418306—
용매TetrahydrofuranHCID 8028—
생성물1-(4-Phenoxyphenyl)prop-2-en-1-olHCID 1970581673%

반응 조건

온도0 °C

반응 단계

tert-Butyllithium (24.5 mL, 1.7M in pentane, 42.2 mmol) was added dropwise over 30 min to a solution of 4-bromodiphenyl ether (5.00 g, 20.1 mmol) in THF (50 mL) at -78° C. under argon. The cooling bath was removed and the bright yellow reaction mixture was warmed to 0° C. over 20 min. The reaction was stirred at 0° C. for 30 min, at which time a tan-colored solution developed. Freshly distilled acrolein (1.6 mL, 24 mmol) was added dropwise over 5 min. The colorless reaction mixture was stirred at 0° C. for 15 min, then quenched by addition of saturated NH4Cl (10 mL). The mixture was diluted with diethyl ether (200 mL) and the organic layer was washed with water (20 mL) and brine (50 mL), then dried over MgSO4. Evaporation gave a crude oil which was purified by flash chromatography on silica gel (400 g) eluted with a step gradient of 10:90 EtOAc/hexane to 15:85 EtOAc/hexane to 20:80 EtOAc/hexane to provide title compound (3.31 g, 73%) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05567841
출처 데이터셋uspto-grants-1996_10
ORD IDord-68936d09f9624790aeab8864ebd585c1
출처 메모uspto-grants-1996_10