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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776279Generated: November 1, 2026

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

https://huagongshe.com/reaction/1776279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2,2-dimethyl-5-(pyridin-4-yl)furan-3(2H)-oneHCID 59354790—
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) 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 numberUS09265767B2
Source datasetuspto-grants-2016_02
ORD IDord-ff3f172606424c068b8a75499ba0c9ff
Source noteuspto-grants-2016_02