HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375384Generated: October 26, 2026
Dimethylformamide → 2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazoline
https://huagongshe.com/reaction/375384
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2(3H)-Thiazolimine, 5-methyl-3-[3-(trifluoromethyl)phenyl]- | HCID 11021546 | — |
| Product | 2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazoline | HCID 11088983 | 91% |
Reaction Steps
A solution of 2-imino-3-(3-trifluoromethylphenyl)-5-methylthiazoline (0.52 g, 2.0 mmol), piperidine (0.51 g, 6.0 mmol) and triethylamine (0.61 g, 6.0 mmol) in N,N-dimethylformamide (10 ml) charged in a reaction flask was reacted with tetrafluoroethylene, which was made to flow intothe flask (ca. 0.3 liter/hr), with vigorous stirring at 50° C. for 9 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 (0.61 g, 1.8 mmol, yield 91%).
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-11d65c1c7a524507b43c6a66b6b3a6a4 |
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| Source note | uspto-grants-1996_01 |
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