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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22029Generated: October 26, 2026

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

https://huagongshe.com/reaction/22029

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-trifluoromethylpheny)-5-bromothiazoline (Compound No. 30).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05426188
Source datasetuspto-grants-1995_06
ORD IDord-e9219addc6ce432f8c50f7527d001711
Source noteuspto-grants-1995_06