HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5317Generated: October 26, 2026
3-(Trifluoromethyl)aniline → Benzenamine, N-2-propyn-1-yl-3-(trifluoromethyl)-
https://huagongshe.com/reaction/5317
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(Trifluoromethyl)aniline | HCID 7375 | — |
| Reactant | Propargyl bromide | HCID 7842 | — |
| Product | Benzenamine, N-2-propyn-1-yl-3-(trifluoromethyl)- | HCID 10488213 | 34.8% |
Reaction Steps
A mixture of 3-trifluoromethylaniline (30 g) ad propargyl bromide (12 g) was stirred at 80° C. for 3 hours, followed by filtration of the reaction mixture. The filtrate was subjected to column chromatography to give N-propargyl-3-trifluoromethylaniline (7 g). A solution of N-propargyl-3-trifluoromethylaniline thus obtained (5.1 g) and ethoxycarbonyl isothiocyalate (3.7 g) in tetrahydrofuran (100 ml) was stirred at room temperature for 8 hours, and the solvent was removed under reduced pressure. The concentrated residue was extracted with chloroform (200 ml), washed with water and dried over anhydrous magnesium sulfate. After removal of the solvent, the residue was subjected to column chromatography to give 5.7 g of 2 -ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine (Compound (i)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05244863 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-d71d3da489d640ec9419ef589183bfc0 |
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| Source note | uspto-grants-1993_09 |
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