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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2(3H)-Thiazolimine, 5-methyl-3-[3-(trifluoromethyl)phenyl]- | HCID 11021546 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazoline | HCID 11088983 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05484933 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-25a335a4b7164a4f9b0146a016db8037 |
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| Source note | uspto-grants-1996_01 |
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