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HRID 1980399생성일: 2026년 10월 26일

Ethyl Bromide → alpha-Ethyl-alpha-(4-chlorophenyl)-4-hydroxy-benzylalcohol

https://huagongshe.com/reaction/1980399

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl BromideHCID 6332—
반응물Ammonium ChlorideHCID 25517—
반응물4-Hydroxy-4'-chlorobenzophenoneHCID 123504—
반응물MagnesiumHCID 5462224—
반응물HCID 178418443HCID 178418443—
용매Diethyl EtherHCID 3283—
생성물alpha-Ethyl-alpha-(4-chlorophenyl)-4-hydroxy-benzylalcoholHCID 14727318—

반응 조건

온도-10 °C

반응 단계

To a solution of ethyl magnesium bromide prepared from 3.9 g. of magnesium turnings and 17.4 g. of ethyl bromide in 50 ml. of dry ether a solution of 9.3 g. of 4-chloro-4'-hydroxy-benzophenone in 40 ml. of dry ether is added dropwise, with stirring at -10° C., in nitrogen atmosphere. The reaction mixture is allowed to warm up to room temperature, stirred at this temperature for an additional half an hour, and is then poured onto a solution of ammonium chloride in ice water 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. After filtering the solvent is distilled off in vacuo, the residue is decolored with charcoal in methanol, the solution is filtered, and the solvent is evaporated under reduced pressure. The crude mixture is crystallized from a mixture of benzene and ethyl acetate to yield 5.5 g. of the named compound, melting at 148° to 149° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04508926
출처 데이터셋uspto-grants-1985_04
ORD IDord-53d61037ce724e43bc1c56f669641de6
출처 메모uspto-grants-1985_04