Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158062Generated: October 31, 2026

N-bromobutanimide → Ethyl 2-bromo-2-(pyridin-4-yl)propanoate

https://huagongshe.com/reaction/1158062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 2-(pyridin-4-yl)propanoateHCID 11651240—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
SolventSodium CarbonateHCID 10340—
ProductEthyl 2-bromo-2-(pyridin-4-yl)propanoateHCID 58930190—

Reaction Steps

The above compounds were prepared according to the procedure reported in the literature: see D. Yang, J. Org. Chem. 2002, 67, 7429. MS: 258, 260 (M+1). To a solution of ethyl 2-(pyridin-4-yl)propanoate (5.3 g, 30 mmol), Mg(ClO4)2 (Aldrich, 2.0 g, 9.0 mmol) in CH3CN (60 mL) was added N-bromosuccinimide (Aldrich, 5.9 g, 33 mmol) at room temperature. After 2 h, the reaction mixture was diluted with ether (200 mL), and 10% Na2CO3. The organic phase was separated, dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography. Mass Spec. m/z+ion 258, 260 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807700B2
Source datasetuspto-grants-2010_10
ORD IDord-efdfa81e5cb045128751cbbed9a88695
Source noteuspto-grants-2010_10