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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375394Generated: October 29, 2026

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

https://huagongshe.com/reaction/375394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantTetrafluoroethyleneHCID 8301—
ReactantSodium CarbonateHCID 10340—
Reactant2(3H)-Thiazolimine, 5-methyl-3-[3-(trifluoromethyl)phenyl]-HCID 11021546—
SolventTolueneHCID 1140—
Product2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazolineHCID 1108898377%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 2-imino-3-(3-trifluoromethylphenyl)-5-methylthiazoline (1.29 g, 5.0 mmol) and piperazine (0.52 g, 6.0 mmol) in toluene (10 ml) charged in a reaction flask was reacted with tetrafluoroethylene, which was made to flow intothe flask (ca. 0.7 liter/hr), with vigorous stirring at 80° C. for 48 hours. After cooling to an ambient temperature, the reaction mixture was poured into saturated aqueous sodium carbonate solution, and extracted with toluene. The toluene 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 (1.29 g, 3.8 mmol, yield 77% ).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484933
Source datasetuspto-grants-1996_01
ORD IDord-eecaf161e47f48ac897a9ede6fbd35a2
Source noteuspto-grants-1996_01