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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426298Generated: November 3, 2026

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

https://huagongshe.com/reaction/2426298

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 numberUS07968560B2
Source datasetuspto-grants-2011_06
ORD IDord-7e705ad8b1bc48ada71bcedc113d85f3
Source noteuspto-grants-2011_06