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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258352Generated: October 30, 2026

N-bromobutanimide → 3-Bromo-2-(pyridin-4-yl)-1-oxaspiro[4.4]non-2-en-4-one

https://huagongshe.com/reaction/1258352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-(Pyridin-4-yl)-1-oxaspiro[4.4]non-2-en-4-oneHCID 59354777—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product3-Bromo-2-(pyridin-4-yl)-1-oxaspiro[4.4]non-2-en-4-oneHCID 5935481072.9%

Reaction Steps

To a stirred solution of afford 2-(pyridin-4-yl)-1-oxaspiro[4.4]non-2-en-4-one (0.18 g, 0.84 mmol) in CHCl3 (10 mL) was added NBS (0.22 g, 1.25 mmol) portionwise at RT and the reaction mixture was stirred for 1 h. The reaction mixture was diluted with DCM (30 mL), washed with water (10 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 3-bromo-2-(pyridin-4-yl)-1-oxaspiro[4.4]non-2-en-4-one (0.18 g, 40%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466148B2
Source datasetuspto-grants-2013_06
ORD IDord-b5e823d05d034642a13e4201f22d0009
Source noteuspto-grants-2013_06