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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975877Generated: October 31, 2026

Triethylamine → Ethyl [2-[4-(4-bromophenyl)-1-piperazinyl]-ethyl]carbamate

https://huagongshe.com/reaction/1975877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 2-chloroethylcarbamateHCID 80621—
Reactant1-(4-Bromophenyl)piperazineHCID 2735629—
SolventDichloromethaneHCID 6344—
ProductEthyl [2-[4-(4-bromophenyl)-1-piperazinyl]-ethyl]carbamateHCID 5443841867.2%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 1-(4-bromophenyl)piperazine (0.018 mol) and ethyl (2-chloroethyl)-carbamate (0.036 mol) was stirred for 2 hours at 130° C. Triethylamine (3 ml) was added and the mixture was stirred for 15 minutes at 130° C. The reaction mixture was cooled to room temperature, CH2Cl2 was added and the resulting mixture was washed with water. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH 95/5). The pure fractions were collected and the solvent was evaporated, yielding 4.3 g (67.2 %) of ethyl [2-[4-(4-bromophenyl)-1-piperazinyl]-ethyl]carbamate (interm. 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06224849B1
Source datasetuspto-grants-2001_05
ORD IDord-089ed39a282c45bb869fd437f0f1d631
Source noteuspto-grants-2001_05