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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910284Generated: October 28, 2026

Ethyl 5-bromopyridine-3-carboxylate → (5-Bromo-3-pyridinyl)methanol

https://huagongshe.com/reaction/910284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-bromopyridine-3-carboxylateHCID 140785—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(5-Bromo-3-pyridinyl)methanolHCID 278473350%

Reaction Steps

A solution of 9 g (40 mmol) of ethyl 5-bromonicotinate in 25 ml of methanol is added dropwise, at room temperature, to a suspension of 14.8 g (400 mmol) of sodium borohydride in 75 ml of methanol. After addition, the reaction medium is refluxed for 2 hours. The reaction medium is evaporated to dryness, taken up in aqueous sodium hydroxide solution to pH 9, and extracted with ethyl acetate. The organic phase is dried over magnesium sulfate, filtered and evaporated under vacuum. 3.7 g (50%) of (5-bromopyrid-3-yl)methanol are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022079B2
Source datasetuspto-grants-2011_09
ORD IDord-49d48d2bdbf5421bba144862e504a0e4
Source noteuspto-grants-2011_09