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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22024Generated: October 29, 2026

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

https://huagongshe.com/reaction/22024

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 numberUS05426188
Source datasetuspto-grants-1995_06
ORD IDord-482e9d172cd34ba28ef8a7bd2430533d
Source noteuspto-grants-1995_06