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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721044Generated: October 26, 2026

3-(Trifluoromethyl)aniline → Benzenamine, N-2-propyn-1-yl-3-(trifluoromethyl)-

https://huagongshe.com/reaction/1721044

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)anilineHCID 7375—
ReactantPropargyl bromideHCID 7842—
ProductBenzenamine, N-2-propyn-1-yl-3-(trifluoromethyl)-HCID 1048821334.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3-trifluoromethylaniline (30 g) and 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508415
Source datasetuspto-grants-1996_04
ORD IDord-dac3ca8fe09c40ec8da64acf8ff61831
Source noteuspto-grants-1996_04