戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1980398作成日:2026年10月27日

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

https://huagongshe.com/reaction/1980398

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-Fluoro-4'-hydroxybenzophenoneHCID 117666—
反応物LithiumHCID 3028194—
反応物HCID 178506846HCID 178506846—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物4-Fluoro-4'-hydroxy-alpha-ethyl-benzhydrolHCID 14727320—

反応条件

温度0 °C

反応手順

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.

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-917d616c80ac4359ad0270951878f8b6
出典メモuspto-grants-1985_04