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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449847Generated: October 26, 2026

Methanol → (3-Allyloxy-pyridin-2-yl)-methanol

https://huagongshe.com/reaction/449847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAllyl bromideHCID 7841—
Reactant3-Hydroxy-2-(hydroxymethyl)pyridine hydrochlorideHCID 3084185—
ReactantSodium MethoxideHCID 10942334—
SolventWaterHCID 962—
Product(3-Allyloxy-pyridin-2-yl)-methanolHCID 1459897762%

Reaction Conditions

Temperature22 °C

Reaction Steps

Hydroxy-2-(hydroxymethyl)pyridine hydrochloride (50 g, 339.6 mmol) and methanol (250 mL) are combined under nitrogen and cooled to 22° C. To the vigorously stirred mixture is added 4.5 M sodium methoxide in MeOH (170.8 mL, 747.2 mmol). The mixture is stirred at room temperature for 2 h and then the solvent is evaporated. The resulting material is dissolved in DMSO (250 mL), allyl bromide (41 g, 339.6 mmoles) is added, and the mixture stirred for 18 h at room temperature. The reaction mixture is added to water (800 mL) and extracted with methylene chloride (3×80 mL). The organic portions are combined and dried over sodium sulfate, filtered, and the solvent evaporated to afford the title compound (34.4 g, 62%). LC-ES/MS m/z 166.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486943B2
Source datasetuspto-grants-2013_07
ORD IDord-3c0e8652eb3f4c2bafbc23a74e5f7fc7
Source noteuspto-grants-2013_07