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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691307Generated: October 30, 2026

Methanol → (6-(Benzyloxy)pyridin-3-yl)methanol

https://huagongshe.com/reaction/1691307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
Reactant6-(Benzyloxy)nicotinaldehydeHCID 21102205—
SolventWaterHCID 962—
Product(6-(Benzyloxy)pyridin-3-yl)methanolHCID 5925513991.1%

Reaction Steps

To a methanol (20.0 mL) solution of 6-benzyloxy-pyridine-3-carbaldehyde (2.00 g, 9.38 mmol) described in Manufacturing Example 12-1-2 was added sodium borohydride (426 mg, 11.3 mmol) on an ice bath (0° C.) under nitrogen atmosphere, which was stirred for 10 minutes at room temperature. Water was added to the reaction mixture at room temperature, which was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure to obtain the title compound (1.84 g, 91.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-2018e4e44d2a49f8b78d07ed9bb0a495
Source noteuspto-grants-2012_04