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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425903Generated: October 31, 2026

N-bromobutanimide → 4-bromo-2,2-dimethyl-5-(thiazol-4-yl)furan-3(2H)-one

https://huagongshe.com/reaction/1425903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2,2-dimethyl-5-(thiazol-4-yl)furan-3(2H)-oneHCID 59354805—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product4-bromo-2,2-dimethyl-5-(thiazol-4-yl)furan-3(2H)-oneHCID 5935485271%

Reaction Steps

To a stirred solution of 2,2-dimethyl-5-(thiazol-4-yl) furan-3(2H)-one (90 mg, 0.46 mmol) in CHCl3 (1.8 mL) was added NBS (0.12 g, 0.69 mmol) portionwise at RT and the reaction mixture was stirred for 1 h. The reaction mixture was diluted with DCM (10 mL), washed with water (5 mL), brine (10 mL), dried over Na2SO4, filtered and then concentrated in vacuo to obtain the crude product. The crude material was purified via silica gel column chromatography to afford 4-bromo-2,2-dimethyl-5-(thiazol-4-yl) furan-3(2H)-one (40 mg, 71%) as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933074B2
Source datasetuspto-grants-2015_01
ORD IDord-a54606957fec48c5b742222194b645df
Source noteuspto-grants-2015_01