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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375393Generated: October 30, 2026

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

https://huagongshe.com/reaction/375393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluoroethyleneHCID 8301—
ReactantAminoethylpiperazineHCID 8795—
ReactantSodium CarbonateHCID 10340—
Reactant2(3H)-Thiazolimine, 5-methyl-3-[3-(trifluoromethyl)phenyl]-HCID 11021546—
SolventDimethylformamideHCID 6228—
Product2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazolineHCID 1108898370%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 2-imino-3-(3-trifluoromethylphenyl)-5-methylthiazoline (1.29 g, 5.0 mmol) and 1-(2-aminoethyl)piperazine (0.78 g, 6.0 mmol) in N,N-dimethylformamide (10 ml) charged in a reaction flask was reacted with tetrafluoroethylene, which was made to flow into the flask (ca. 0.7 liter/hr), with vigorous stirring at 50° C. for 33 hours. After cooling to an ambient temperature, the reaction mixture was poured into saturated aqueous sodium carbonate solution, and extracted with diethyl ether. The diethyl ether 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 (1.18 g, 3.5 mmol, yield 70%). Unreacted part of 2-imino-3-(3-trifluoromethylphenyl)-5-methylthiazoline (0.12 g) was recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484933
Source datasetuspto-grants-1996_01
ORD IDord-7a6ab38ecbab496ab43f0e31b0c5f382
Source noteuspto-grants-1996_01