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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396708Generated: October 31, 2026

Trifluoroacetic acid → 2-(4-Chlorophenoxy)-1-(piperazin-1-yl)ethanone

https://huagongshe.com/reaction/1396708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-(2-(4-chlorophenoxy)acetyl)piperazine-1-carboxylateHCID 50941486—
SolventDichloromethaneHCID 6344—
Product2-(4-Chlorophenoxy)-1-(piperazin-1-yl)ethanoneHCID 1074760736.1%

Reaction Steps

A suspension of tert-butyl 4-(2-(4-chlorophenoxy)acetyl)piperazine-1-carboxylate (example 58, 0.58 g, 0.16 mmol) in dichloromethane (8 ml) was treated dropwise at room temperature with TFA until the solid completely dissolved. The reaction mixture was stirred under nitrogen at room temperature overnight. The volatiles were evaporated to dryness, diluted with water and the solid was collected by filtration. The solid was washed with water and dried to yield the title compound as a white solid (0.30 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901132B2
Source datasetuspto-grants-2014_12
ORD IDord-e2433aad94064d38a033be1348bee1db
Source noteuspto-grants-2014_12