Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721052Generated: October 27, 2026

1,1-Dibromoethane → 2-Imino-3-(3-trifluoromethylphenyl)thiazolidine

https://huagongshe.com/reaction/1721052

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DibromoethaneHCID 11201—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Trifluoromethyl)phenylthioureaHCID 735844—
SolventAcetoneHCID 180—
Product2-Imino-3-(3-trifluoromethylphenyl)thiazolidineHCID 22416978110%

Reaction Steps

A solution of N-(3-trifluoromethylphenyl)thiourea (6.1 g), dibromoethane (5.7 g) and anhydrous potassium carbonate (11.5 g) in acetone (60 ml) was refluxed for 1 day. The solvent was removed by distillation therefrom, and the residue was extracted with ethyl ether, washed with water, dried over anhydrous magnesium sulfate and subjected to column chromatography to give 7.5 g of 2-imino-3-(3-trifluoromethylphenyl)thiazolidine. The thus obtained 2-imino-3- (3-trifluoromethylphenyl) thiazolidine (1.0 g), n-butyl chlorocarbonate (0.61 g) and triethylamine (1.2 g) were dissolved in tetrahydrofuran, and the resultant solution was stirred at room teperature for 5 hours. The solvent was removed, and the residue was extracted with ethyl acetate, washed with water and dried over anhydrous magnesium sulfate. After removal of the solvent, the residue was subjected to column chromatography to give 0.57 g of 2-butoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508415
Source datasetuspto-grants-1996_04
ORD IDord-43d0f27c12c44a1592467de301b85f2a
Source noteuspto-grants-1996_04