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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551729Generated: October 31, 2026

4-Methoxyphenol → 4-Methoxyphenol

https://huagongshe.com/reaction/551729

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxyphenolHCID 9015—
ReactantTriphenylphosphineHCID 11776—
Reactant2,4-Pentanediol, (-)-HCID 2723683—
Reactant2-methoxyethyl N-(2-methoxyethoxycarbonylimino)carbamateHCID 53384415—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-MethoxyphenolHCID 9015—
Product(4S,2R)-4-(4-methoxyphenoxy)pentane-2-olHCID 59202686—

Reaction Steps

After 4-methoxyphenol (300 mg, 2.41 mmol), triphenylphosphine (761 mg, 2.89 mmol), (2R,4R)-2,4-pentanediol (302 mg, 2.89 mmol), and THF (12 mL) were added to a 50 ml flask, azodicarboxylic acid bis(2-methoxyethyl) ester (680 mg, 2.89 mmol) dissolved in THF (6 ml) was added dropwise thereto at 20° C., and the reaction was allowed to proceed for 14 hours. Water (0.5 ml) was added, and concentration was carried out. Then, water (10 ml) was added to the solution, and extraction was carried out using diethyl ether (10 mL, ×2). Then, the organic layer was washed with water (10 ml) and saturated salt water (10 ml), and dehumidified with anhydrous magnesium sulfate. Subsequently, a crude product obtained by concentration was purified by column chromatography (silica gel, 30% ethyl acetate-hexane solution) to give (4S,2R)-4-(4-methoxyphenoxy)pentane-2-ol as a colorless oily substance (418 mg, yield: 82%/4-methoxyphenol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947816B2
Source datasetuspto-grants-2011_05
ORD IDord-5b673362c90b42368dc925fea609f2f8
Source noteuspto-grants-2011_05