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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972353Generated: November 1, 2026

Acetonitrile → 2,2,2-Trifluoro-1-(4-(4-(phenylsulfonyl)-1-piperazinyl)phenyl)ethanone

https://huagongshe.com/reaction/1972353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTriethylamineHCID 8471—
Reactant2,2,2,4'-TetrafluoroacetophenoneHCID 69564—
Reactant1-(Benzenesulfonyl)piperazine hydrochlorideHCID 2756581—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product2,2,2-Trifluoro-1-(4-(4-(phenylsulfonyl)-1-piperazinyl)phenyl)ethanoneHCID 6658235750.9%

Reaction Conditions

Temperature110 °C

Reaction Steps

A 125 ml, pressure tube was charged with 2,2,2-trifluoro-1-(4-fluorophenyl)ethanone (7.31 g, 38.1 mmol, Sigma-Aldrich, St. Louis, Mo.), 1-(phenylsulfonyl)piperazine hydrochloride (5.00 g, 19.0 mmol), 20 mL of CH3CN, and triethylamine (7.96 mL, 57.1 mmol). The tube was sealed and heated at 110° C. for 3 h. After that time, the mixture was diluted with EtOAc (100 mL) and water (50 mL). The organics were separated, dried (MgSO4) and concentrated to give a white solid. This solid was slurried with hexane (150 mL) to give 2,2,2-trifluoro-1-(4-(4-(phenylsulfonyl)-1-piperazinyl)phenyl)ethanone (3.85 g) as a bright white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431563B2
Source datasetuspto-grants-2013_04
ORD IDord-e46e3af9d2f84f04901fd03ab92c2018
Source noteuspto-grants-2013_04