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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742453Generated: October 25, 2026

Trifluoroacetic acid → Trifluoroacetamidoacetone

https://huagongshe.com/reaction/1742453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-Propanone, 1-amino-, hydrochlorideHCID 3084025—
SolventDichloromethaneHCID 6344—
ProductTrifluoroacetamidoacetoneHCID 14076243—

Reaction Steps

Aminoacetone hydrochloride (13.29 g, 121 mmol) was slurried in 200 mL of dichloromethane and stirred vigorously as 22 mL (146 mmol) of trifluoroacetic acid was added. The mixture was heated to reflux with stirring for about 1 hour at which time the evolution of gas had ceased. The resulting mixture was concentrated by evaporation at 60° C. and the residue was dissolved in 200 mL of ether. Solid sodium bicarbonate was cautiously added with stirring until foaming ceased. The resulting slurry was filtered through a 2×5 cm silica gel plug and the plug was eluted with an additional 100 mL of ether. The combined filtrates were concentrated by evaporation at temperatures up to 60° C. The residue was kugelrohr distilled at a pot temperature of 100°-110° C. and a pressure of 18 torr (2.4 kPa) to obtain 9.7 g (47 percent of theory) of the title compound as a waxy white solid. An analytical sample prepared by recrystallization from pentane was a white solid melting at 71°-73° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05338856
Source datasetuspto-grants-1994_08
ORD IDord-127d11c180a040bb8b80ae2b5d47becf
Source noteuspto-grants-1994_08