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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1980398생성일: 2026년 10월 27일

Ethyl Bromide → 4-Fluoro-4'-hydroxy-alpha-ethyl-benzhydrol

https://huagongshe.com/reaction/1980398

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl BromideHCID 6332—
반응물Ammonium ChlorideHCID 25517—
반응물4-Fluoro-4'-hydroxybenzophenoneHCID 117666—
반응물LithiumHCID 3028194—
반응물HCID 178506846HCID 178506846—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물4-Fluoro-4'-hydroxy-alpha-ethyl-benzhydrolHCID 14727320—

반응 조건

온도0 °C

반응 단계

To a solution of ethyl lithium prepared from 2.8 g. of lithium metal and 21.8 g. of ethyl bromide in 265 ml. of dry ether a solution of 10.8 g. of 4-fluoro-4'-hydroxy-benzophenone in 50 ml. of dry tetrahydrofurane is added dropwise, with stirring in argon atmosphere, at a temperature between -40° C. and -30° C. When the addition is complete, the mixture is allowed to warm up to 0° C., and is then stirred at this temperature for further 30 minutes. The mixture is decomposed with a 20% aqueous ammonium chloride solution under cooling. The aqueous phase is extracted with ether, the ethereal phases are combined, washed to neutral with water, and dried over anhydrous magnesium sulfate. The solution is evaporated under reduced pressure, and the solid residue is crystallized from a mixture of n-hexane and ethyl acetate to yield 8.2 g. of the named product, melting at 125° to 126° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04508926
출처 데이터셋uspto-grants-1985_04
ORD IDord-917d616c80ac4359ad0270951878f8b6
출처 메모uspto-grants-1985_04