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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375398Generated: October 29, 2026

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

https://huagongshe.com/reaction/375398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTetrafluoroethyleneHCID 8301—
ReactantSodium BicarbonateHCID 516892—
Reactant2(3H)-Thiazolimine, 5-methyl-3-[3-(trifluoromethyl)phenyl]-HCID 11021546—
SolventAcetonitrileHCID 6342—
Product2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazolineHCID 1108898376%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 2-imino-3-(3-trifluoromethylphenyl)-5-methylthiazoline (0.64 g, 2.5 mmol) and morpholine (0.48 g, 5.5 mmol) in acetonitrile (5 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 50° C. for 13 hours. After cooling to an ambient temperature, the reaction solution was poured intoa saturated aqueous sodium hydrogen-carbonate solution (50 ml), and extracted twice with toluene (50 ml×2). The toluene layer was washed twice with 5% hydrochloric acid (30 ml×2) and water (50 ml) and then brine (50 ml), 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 (0.64 g, 1.9 mmol, yield 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484933
Source datasetuspto-grants-1996_01
ORD IDord-25a335a4b7164a4f9b0146a016db8037
Source noteuspto-grants-1996_01