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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375395Generated: October 25, 2026

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

https://huagongshe.com/reaction/375395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTetrafluoroethyleneHCID 8301—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Imino-3-(3-trifluoromethyl-phenyl)-5-methylthiazoline hydrochlorideHCID 21480071—
SolventDimethylformamideHCID 6228—
Product2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazolineHCID 1108898387%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 2-imino-3-(3-trifluoromethylphenyl)-5-methylthiazoline hydrochloride (1.47 g, 5.0 mmol) and morpholine (1.57 g, 18.0 mmol) in N,N-dimethylformamide (10 ml) charged in a reaction flask was reacted with tetrafluoroethylene, which was made to flow intothe flask (ca. 0.7 liter/hr), with vigorous stirring at 60° C. for 2 hours. After cooling to an ambient temperature, the reaction mixture was poured into 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 (70 ml) and then brine (70 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 (1.47 g, 4.4 mmol, yield 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484933
Source datasetuspto-grants-1996_01
ORD IDord-d7dcdc96c83a4b3abad24f5941865b01
Source noteuspto-grants-1996_01