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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864571Generated: October 30, 2026

Sodium borohydride → (6-Iodopyridin-3-yl)methanol

https://huagongshe.com/reaction/1864571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl6-iodonicotinoateHCID 10891136—
SolventEthanolHCID 702—
Product(6-Iodopyridin-3-yl)methanolHCID 2303951667%

Reaction Conditions

Temperature0 °C

Reaction Steps

30 g (108 mmol) of ethyl 6-iodonicotinate dissolved in 300 ml of ethanol are added dropwise to a solution of 20.5 g (542 mmol) of sodium borohydride in 200 ml of ethanol, cooled beforehand to 0° C. The reaction medium is allowed to warm to room temperature and is then stirred for 1 hour 30 minutes at room temperature. The reaction medium is hydrolysed and extracted with ethyl acetate. The boron salts precipitate out, and the medium is filtered and then evaporated to dryness. The reaction medium is taken up in dichloromethane, the product precipitates out, isopropyl ether is added and the medium is filtered. The precipitate is washed with isopropyl ether. 17 g (67%) of (6-iodopyrid-3-yl)methanol are obtained in the form of a pale yellow solid with a melting point of 102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625914B2
Source datasetuspto-grants-2009_12
ORD IDord-de2e2c6d229048b58e8e118aba2a180b
Source noteuspto-grants-2009_12