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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655444Generated: October 30, 2026

N-bromobutanimide → HCID 59354811, compound

https://huagongshe.com/reaction/655444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 59354856HCID 59354856—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 59354811HCID 5935481169%

Reaction Steps

To a stirred solution of 5-(benzo[c][1,2,5]thiadiazol-5-yl)-2,2-dimethylfuran-3(2H)-one (0.5 g, 2.164 mmol) in CHCl3 (15 mL), NBS (0.462 g, 2.590 mmol) was added portionwise at RT. The reaction mixture was then stirred for 2 h and diluted with DCM (10 mL). The combined organic layers were washed with water (5 mL) and 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 5-(benzo[c][1,2,5]thiadiazol-5-yl)-4-bromo-2,2-dimethylfuran-3(2H)-one (0.45 g, 69%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071595B2
Source datasetuspto-grants-2011_12
ORD IDord-f6f4842e31a34ac9a7663519bb4336f4
Source noteuspto-grants-2011_12