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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578750Generated: October 30, 2026

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

https://huagongshe.com/reaction/578750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 5-bromopyridine-2-carboxylateHCID 7016458—
SolventEthanolHCID 702—
Product(5-Bromopyridin-2-yl)methanolHCID 5200169—

Reaction Steps

Methyl 5-bromopyridine-2-carboxylate (2.00 g, 9.27 mmol) was dissolved in ethanol (20.0 mL). Sodium borohydride (1.05 g, 27.8 mmol) was added at 0° C., and the mixture was stirred at room temperature for 18 h. The mixture was then concentrated under reduced pressure, quenched with 1 N hydrochloric acid, neutralized with solid potassium carbonate and extracted with dichloromethane. The organic layer was dried over magnesium sulfate and evaporated to give 1.57 g (90% of th.) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040691B2
Source datasetuspto-grants-2015_05
ORD IDord-da26f20938424b4e8d715b0b9da26a96
Source noteuspto-grants-2015_05