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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506862Generated: November 4, 2026

Trifluoroacetic acid → 1-[4-(Trifluoromethoxy)benzenesulfonyl]piperazine

https://huagongshe.com/reaction/506862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-(4-Trifluoromethoxy-benzenesulfonyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 45862930—
SolventDichloromethaneHCID 6344—
Product1-[4-(Trifluoromethoxy)benzenesulfonyl]piperazineHCID 207940287%

Reaction Steps

To a cold (0 C) solution of 4-(4-trifluoromethoxy-benzenesulfonyl)-piperazine-1-carboxylic acid tert-butyl ester (1.15 g, 2.8 mmol) in DCM (3 ml) was added TFA (2 ml). The resulting solution was stirred for 1 hr. Solvent was then removed under reduced pressure. The crude solid was taken-up in AcOEt (15 ml) and washed with NaHCO3 sat (2×5 ml), water (5 ml) and finally with brine (5 ml). The organic layer was dried over MgSO4 and the solvent was removed under vacuo to yield the desired 1-(4-trifluoromethoxy-benzenesulfonyl)-piperazine as a white solid (753 mg, 87% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786121B2
Source datasetuspto-grants-2010_08
ORD IDord-9c44250bc06b4969abc709fb7e3ae94f
Source noteuspto-grants-2010_08