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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721036Generated: October 31, 2026

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

https://huagongshe.com/reaction/1721036

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-methylthiazolineHCID 5380341864%

Reaction Steps

A solution of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-bromomethylthiazolidine (0.7 g) and potassium t-butoxide (0.25 g) in t-butanol (30 ml) was refluxed for 5 hours. After removal of the solvent under reduced pressure, the concentrated residue was extracted with chlorofom (100 ml), washed with water and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was subjected to column chromatography to give 0.36 g of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-methylthiazoline (Compound No. 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508415
Source datasetuspto-grants-1996_04
ORD IDord-270da6a342fa465a9fd3a8cf07307212
Source noteuspto-grants-1996_04