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HRID 1980399作成日:2026年10月26日

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

https://huagongshe.com/reaction/1980399

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl BromideHCID 6332—
反応物Ammonium ChlorideHCID 25517—
反応物4-Hydroxy-4'-chlorobenzophenoneHCID 123504—
反応物MagnesiumHCID 5462224—
反応物HCID 178418443HCID 178418443—
溶媒Diethyl EtherHCID 3283—
生成物alpha-Ethyl-alpha-(4-chlorophenyl)-4-hydroxy-benzylalcoholHCID 14727318—

反応条件

温度-10 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04508926
出典データセットuspto-grants-1985_04
ORD IDord-53d61037ce724e43bc1c56f669641de6
出典メモuspto-grants-1985_04