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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Chloro-1-(6-chloropyridin-3-yl)ethanone | HCID 10797730 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-Bromo-1-(6-chloropyridin-3-YL)ethanone | HCID 19432921 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Chloro-5-(oxiran-2-yl)pyridine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802673B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-be1242b5688244adbe5d119921d71f82 |
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| Source note | uspto-grants-2014_08 |
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