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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798677Generated: October 28, 2026

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

https://huagongshe.com/reaction/1798677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2,2-dimethyl-5-(pyridin-4-yl)furan-3(2H)-oneHCID 59354790—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product4-bromo-2,2-dimethyl-5-(pyridin-4-yl)furan-3(2H)-oneHCID 5935482421.8%

Reaction Steps

To a stirred solution of 2,2-dimethyl-5-(pyridin-4-yl) furan-3(2H)-one (0.81 g, 4.28 mmol) in CHCl3 (20 mL), NBS (1.3 g, 7.28 mmol) was added portionwise at RT. The reaction mixture was then stirred for 2 h and diluted with DCM (100 mL). The organic layers were washed with water (50 mL) and brine (50 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-(pyridin-4-yl) furan-3(2H)-one (0.25 g, 21%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343973B2
Source datasetuspto-grants-2013_01
ORD IDord-a4a52d10af274f458ca0acc2f6649996
Source noteuspto-grants-2013_01