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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389278Generated: October 26, 2026

1-Piperazinecarboxylic acid, ethyl ester → Ethyl 4-[2-(4-fluorophenyl)ethyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/1389278

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Piperazinecarboxylic acid, ethyl esterHCID 8431—
Reactant4-Fluorophenethyl bromideHCID 573153—
SolventWaterHCID 962—
ProductEthyl 4-[2-(4-fluorophenyl)ethyl]piperazine-1-carboxylateHCID 1267985891%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 80 g 1-(ethoxycarbonyl)piperazine and 41 g of 2-(4-fluorophenyl)ethyl bromide is kept at room temperature overnight and then heated to 100° C. for 1 hour. After cooling, it is diluted with 50 ml water and extracted with benzene. The extract is washed with water and then shaken with 5% hydrochloric acid. The separated solid hydrochloride is filtered off, washed with a small quantity of water, decomposed by treatment with aqueous ammonia and the base isolated again by extraction with benzene. Processing of the extract affords 51 g (91%) of the crude 1-(ethoxycarbonyl)-4-(2-[4-fluorophenyl]ethyl)piperazine, b.p. 198° C./3 Torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04243805
Source datasetuspto-grants-1981_01
ORD IDord-c7a1a6380ce448c7853ba59a71e45744
Source noteuspto-grants-1981_01