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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074236Generated: October 31, 2026

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

https://huagongshe.com/reaction/2074236

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 numberUS07919494B2
Source datasetuspto-grants-2011_04
ORD IDord-6074e52adb22490c877e928fb7edcc22
Source noteuspto-grants-2011_04