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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721054Generated: October 26, 2026

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

https://huagongshe.com/reaction/1721054

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DibromoethaneHCID 11201—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl N-{[3-(trifluoromethyl)phenyl]carbamothioyl}carbamateHCID 971062—
SolventAcetoneHCID 180—
Product2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidineHCID 5422583383.1%

Reaction Steps

A solution of N-(3-trifluoromethylphenyl)-N'-ethoxycarbonylthiourea (1.8 g), dibromoethane (1.29 g) and anhydrous potassium carbonate (2.6 g) in acetone (20 ml) was refluxed for 5 hours. The solvent was removed by distillation, and the residue was extracted with diethyl ether. The extract was washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized from a mixture of hexane and ethanol to give 1.63 g of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidine. m.p., 75.8° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508415
Source datasetuspto-grants-1996_04
ORD IDord-3c6dc74784c848f895598dd8e3f3e02a
Source noteuspto-grants-1996_04