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HRID 41693作成日:2026年10月25日

Triethylamine → Benzyl 4-(4-bromophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/41693

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Benzyl chloroformateHCID 10387—
反応物1-(4-Bromophenyl)piperazineHCID 2735629—
溶媒DichloromethaneHCID 6344—
生成物Benzyl 4-(4-bromophenyl)piperazine-1-carboxylateHCID 46739494—

反応手順

5 g of 4-bromophenylpiperazine are placed in a 500 ml three-necked flask under a nitrogen atmosphere. 4.34 ml of triethylamine are added. The mixture is cooled in an ice bath and 3.24 ml of benzyl chloroformate are added. The mixture is allowed to return to ambient temperature. It is diluted with dichloromethane and then gentle hydrolysis is carried out. The aqueous phase is extracted with dichloromethane. The organic phases are combined, washed with a saturated NaCl solution, dried over sodium sulphate, then filtered through a sintered glass filter and concentrated under vacuum. 8.43 g of 4-(4-bromophenyl)piperazine-1-carboxylic acid benzyl ester are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530657B2
出典データセットuspto-grants-2013_09
ORD IDord-c53fbf5f16654f649222fece5a7bfb47
出典メモuspto-grants-2013_09