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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403289Generated: November 1, 2026

Sodium borohydride → 2-Chloro-5-(oxiran-2-yl)pyridine

https://huagongshe.com/reaction/2403289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-Chloro-1-(6-chloropyridin-3-yl)ethanoneHCID 10797730—
ReactantSodium MethoxideHCID 10942334—
Reactant2-Bromo-1-(6-chloropyridin-3-YL)ethanoneHCID 19432921—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product2-Chloro-5-(oxiran-2-yl)pyridineHCID 22171351—

Reaction Steps

To a stirred solution of the mixture of 2-bromo-1-(6-chloropyridin-3-yl)ethanone and 2-chloro-1-(6-chloropyridin-3-yl)ethanone (5.6 g) in ethanol (100 ml) at 5° C. was added portionwise over 5 min NaBH4 (904 mg). The reaction mixture was then stirred at room temperature for 1 hour to afford a light yellow solution. TLC analysis showed the reaction was complete. Sodium methoxide (645 mg) was then added and the reaction mixture was stirred at room temperature overnight. TLC analysis showed a small amount of starting material remaining and so the reaction mixture was stirred at 50° C. for 1 h. The reaction mixture was then poured into EtOAc and washed with saturated brine. The organic phase was dried over Na2SO4 and concentrated in vacuo to afford (RS)-2-chloro-5-(oxiran-2-yl)pyridine (4.04 g) as a yellow oil which was used in the next step without further purification. MS (ISP): 158.0 ([{37Cl}M+H]+), 156.0 ([{35Cl}M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802673B2
Source datasetuspto-grants-2014_08
ORD IDord-be1242b5688244adbe5d119921d71f82
Source noteuspto-grants-2014_08