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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694155Generated: November 1, 2026

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

https://huagongshe.com/reaction/1694155

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 numberUS08158657B2
Source datasetuspto-grants-2012_04
ORD IDord-9d7efa798c8049879e38e7743a456709
Source noteuspto-grants-2012_04