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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22032Generated: October 30, 2026

Potassium tert-butoxide → 2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine

https://huagongshe.com/reaction/22032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-bromomethylthiazolidineHCID 53634945—
Solventtert-ButanolHCID 6386—
Product2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidineHCID 5403846444.5%

Reaction Steps

A.solution of 2-ethoxycarbonylimino-3-(3-tri-fluoromethylphenyl)-5-bromomethylthiazolidine (0.7 g) and potassium t-butoxide (0.25 g) in t-butanol (30 ml) was refluxed for 5 hours, and the solvent was distilled off under reduced pressure. The residue was extracted with chloroform (100 ml), washed with water and dried over anhydrous magnesium sulfate. After removal of the solvent, the residue was subjected to column chromatography to give 0.25 g of 2-ethoxycarbonylimino-3-(3-trifluoromethyl-phenyl)-5-methylenethiazolidine (Compound (i)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05426188
Source datasetuspto-grants-1995_06
ORD IDord-5505bdf514d3417f835495e1e3c4378c
Source noteuspto-grants-1995_06