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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721042Generated: October 25, 2026

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

https://huagongshe.com/reaction/1721042

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 numberUS05508415
Source datasetuspto-grants-1996_04
ORD IDord-29f33485db5844ac8296bc2d529b5278
Source noteuspto-grants-1996_04