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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5315Generated: October 25, 2026

N-bromobutanimide → 2-Ethoxycarbonylimino-3-(3-trifluoromethylpheny)-5-bromothiazoline

https://huagongshe.com/reaction/5315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Ethoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidineHCID 54225833—
SolventChloroformHCID 6212—
Product2-Ethoxycarbonylimino-3-(3-trifluoromethylpheny)-5-bromothiazolineHCID 5409699345.3%

Reaction Steps

A solution of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidine (1.6 g) and N-bromosuccinimide (2 g) in chloroform (50 ml) was refluxed for 10 hours. After cooling, the reaction mixture was washed with an aqueous sodium sulfite solution and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was subjected to column chromatography to give 0.9 g of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-bromothiazoline (Compound No. 30).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244863
Source datasetuspto-grants-1993_09
ORD IDord-be24221918f44d34a8f5c8d9a0afeeda
Source noteuspto-grants-1993_09