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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375384Generated: October 26, 2026

Dimethylformamide → 2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazoline

https://huagongshe.com/reaction/375384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPiperidineHCID 8082—
ReactantTetrafluoroethyleneHCID 8301—
ReactantTriethylamineHCID 8471—
Reactant2(3H)-Thiazolimine, 5-methyl-3-[3-(trifluoromethyl)phenyl]-HCID 11021546—
Product2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazolineHCID 1108898391%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 2-imino-3-(3-trifluoromethylphenyl)-5-methylthiazoline (0.52 g, 2.0 mmol), piperidine (0.51 g, 6.0 mmol) and triethylamine (0.61 g, 6.0 mmol) in N,N-dimethylformamide (10 ml) charged in a reaction flask was reacted with tetrafluoroethylene, which was made to flow intothe flask (ca. 0.3 liter/hr), with vigorous stirring at 50° C. for 9 hours. After cooling to an ambient temperature, the reaction mixture was poured into ice-water, and extracted with ethyl acetate. The ethyl acetate layer was washed with water and then brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was subjected to silica gel column chromatography, which afforded 2-difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazoline (0.61 g, 1.8 mmol, yield 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484933
Source datasetuspto-grants-1996_01
ORD IDord-11d65c1c7a524507b43c6a66b6b3a6a4
Source noteuspto-grants-1996_01