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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605788Generated: November 3, 2026

Methanol → 6-(Methoxymethyl)pyridin-3-ol

https://huagongshe.com/reaction/605788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 10639974HCID 10639974—
ReactantSodium MethoxideHCID 10942334—
SolventWaterHCID 962—
Product6-(Methoxymethyl)pyridin-3-olHCID 2314577559%

Reaction Steps

Sodium methoxide (393 mg) was added to a methanol (20 ml) solution containing 5-(benzenesulfonyloxy)-2-(bromomethyl)pyridine (Beilstein Registry No. 7430370, 800 mg), followed by stirring at room temperature for 4 hours. Water was added to the reaction solution, followed by extraction with EtOAc. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: EtOAc) to obtain 6-(methoxymethyl)pyridin-3-ol (200 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915261B2
Source datasetuspto-grants-2011_03
ORD IDord-cd04bd46ad394ab290424b511752cf98
Source noteuspto-grants-2011_03