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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666388Generated: October 26, 2026

3-Hydroxybenzyl alcohol → 3-[(6-Methyl-2-pyridinyl)oxy]benzenemethanol

https://huagongshe.com/reaction/1666388

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Hydroxybenzyl alcoholHCID 102—
ReactantCesium carbonateHCID 10796—
Reactant2-Fluoro-6-methylpyridineHCID 96090—
SolventDimethyl SulfoxideHCID 679—
Product3-[(6-Methyl-2-pyridinyl)oxy]benzenemethanolHCID 6687611464%

Reaction Conditions

Temperature110 °C

Reaction Steps

3-Hydroxymethyl-phenol (3.69 g, 29.7 mmol), 2-fluoro-6-methyl-pyridine (3.00 g, 27 mmol,) and cesium carbonate (9.68 g, 29.7 mmol) were suspended in dimethylsulfoxide (25 mL) and heated to 110° C. After stirring for 16 h, the reaction was partitioned between water (250 mL) and ethyl acetate (250 mL). The organic layer was separated and the aqueous was extracted again with ethyl acetate. The combined organic layer was dried over sodium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography (10-50%, EtOAc:heptane) to afford the title compound (3.72 g, 64% yield) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044052B2
Source datasetuspto-grants-2011_10
ORD IDord-9ea66b4dec644cb4a889b38fdfe4acff
Source noteuspto-grants-2011_10