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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507789Generated: November 1, 2026

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

https://huagongshe.com/reaction/1507789

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 numberUS09221822B2
Source datasetuspto-grants-2015_12
ORD IDord-8224aa2ae0764333ad03d05fa7b748e2
Source noteuspto-grants-2015_12