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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175240Generated: October 29, 2026

Sodium borohydride → (5-Bromopyridin-2-yl)methanol

https://huagongshe.com/reaction/2175240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 5-bromopicolinateHCID 12686158—
SolventMethanolHCID 887—
Product(5-Bromopyridin-2-yl)methanolHCID 520016980%

Reaction Steps

To a solution of NaBH4 (0.822 g, 21.73 mmol) in MeOH (25 mL) was added ethyl 5-bromopicolinate (1.0 g, 4.35 mmol) portion-wise over a period of 10 min at room temperature. The mixture was stirred at room temperature for 10 min and then heated to 70° C. for 30 min. The solvent was removed in vacuo, and the resulting residue was diluted with EtOAc and water. The aqueous phase was adjusted to pH 7 with 1 N aq. HCl, and extracted with EtOAc. The combined organic layer was dried over MgSO4, filtered, and concentrated in vacuo to afford the title compound (0.65 g, 80% yield) as a white solid. LCMS, [M+H]+=187.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062028B2
Source datasetuspto-grants-2015_06
ORD IDord-be7824b77be74e21a356cd55e420f277
Source noteuspto-grants-2015_06