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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891911Generated: November 2, 2026

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

https://huagongshe.com/reaction/1891911

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 numberUS08507530B2
Source datasetuspto-grants-2013_08
ORD IDord-a1392231f5a54b05a6583a40a2e52cd1
Source noteuspto-grants-2013_08