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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425864Generated: October 31, 2026

N-bromobutanimide → HCID 59354811, compound

https://huagongshe.com/reaction/1425864

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 numberUS08933074B2
Source datasetuspto-grants-2015_01
ORD IDord-d7cd43d2910246b1bb772f74b051decf
Source noteuspto-grants-2015_01