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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375396Generated: October 28, 2026

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

https://huagongshe.com/reaction/375396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTetrafluoroethyleneHCID 8301—
ReactantSodium BicarbonateHCID 516892—
Reactant2(3H)-Thiazolimine, 5-methyl-3-[3-(trifluoromethyl)phenyl]-HCID 11021546—
SolventDimethylformamideHCID 6228—
Product2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazolineHCID 1108898398%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 2-imino-3-(3-trifluoromethylphenyl)-5-methylthiazoline (1.29 g, 5.0 mmol) and morpholine (0.96 g, 11.0 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 13 hours. After cooling to an ambient temperature, the reaction mixture was poured into a saturated aqueous sodium hydrogencarbonate solution (100 ml), and extracted twice with toluene (100 ml×2). The toluene layer was washed twice with 5% hydrochloric acid (50 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 (1.64 g, 4.9 mmol, yield 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484933
Source datasetuspto-grants-1996_01
ORD IDord-54e67a2266b5454486e77d1eef3e31d4
Source noteuspto-grants-1996_01