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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776377Generated: November 2, 2026

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

https://huagongshe.com/reaction/1776377

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 numberUS09265767B2
Source datasetuspto-grants-2016_02
ORD IDord-19cd175334f74d2689db328ce200e44f
Source noteuspto-grants-2016_02