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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41693Generated: October 25, 2026

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

https://huagongshe.com/reaction/41693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
Reactant1-(4-Bromophenyl)piperazineHCID 2735629—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4-(4-bromophenyl)piperazine-1-carboxylateHCID 46739494—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530657B2
Source datasetuspto-grants-2013_09
ORD IDord-c53fbf5f16654f649222fece5a7bfb47
Source noteuspto-grants-2013_09