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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165706Generated: November 1, 2026

Dimethyl Sulfoxide → 2-(Trifluoromethyl)piperazine

https://huagongshe.com/reaction/2165706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant3-Bromo-1,1,1-trifluoro-2-propanoneHCID 79008—
ReactantSodium borohydrideHCID 4311764—
ReactantN1,N1-Dibenzylethane-1,2-diamineHCID 6394114—
SolventEthanolHCID 702—
Product2-(Trifluoromethyl)piperazineHCID 18519725—

Reaction Steps

A 12.3 g portion of bromo-3,3,3-trifluoropropanone was slowly added to 50 ml of dimethyl sulfoxide and stirred under a dry atmosphere for 21 hours and then diluted to 100 ml with ethanol. A solution of 31 g of N,N-dibenzylethylenediamine in 100 ml of ethanol was added dropwise and the mixture was stirred for 8 hours. A 2.43 g portion of sodium borohydride was added over 30 minutes, this mixture was stirred overnight then the ethanol was removed. The dimethyl sulfoxide residue was dissolved in water and extracted with dichloromethane. The extracts were combined, washed with water and brine and then subjected to flash chromatography on a silica gel column, eluting with ether:hexane (3:7). The 2-(trifluoromethyl)dibenzylpiperazine was dissolved in 25 ml of ethanol in an argon flushed Parr bottle. A 0.63 g portion of 10% palladium on carbon was added and the mixture was shaken under 47 lbs. of hydrogen pressure overnight at 40° C. Filtration and evaporation of the solvent gave 0.55 g of 2-(trifluoromethyl)piperazine as a semi-solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04940710
Source datasetuspto-grants-1990_07
ORD IDord-df3d4ad9f0174de588aff5c9cce70a91
Source noteuspto-grants-1990_07