HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375388Generated: October 26, 2026
Diethylamine → 2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazoline
https://huagongshe.com/reaction/375388
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2(3H)-Thiazolimine, 5-methyl-3-[3-(trifluoromethyl)phenyl]- | HCID 11021546 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazoline | HCID 11088983 | 53% |
Reaction Steps
A solution of 2-imino-3-(3-trifluoromethylphenyl)-5-methylthiazoline (0.77 g, 3.0 mmol), diethylamine (1.32 g, 18.0 mmol) and potassium carbonate (1.04 g, 7.5 mmol) in N,N-dimethylformamide (15 ml) charged in a reaction flask was reacted with tetrafluoroethylene, which was made to flow intothe flask (ca. 0.3 liter/hr), with vigorous stirring at 50° C. for 32 hours. After cooling to an ambient temperature, the reaction mixture was poured into ice-water, and extracted with ethyl acetate. The ethyl acetate 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 (0.53 g, 1.6 mmol, yield 53%).
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-46d15256819f4fc28fd5ae4326fc819f |
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| Source note | uspto-grants-1996_01 |
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