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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162867Generated: October 28, 2026

4-Methoxyphenol → 4-Methoxyphenol

https://huagongshe.com/reaction/1162867

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 numberUS07820802B2
Source datasetuspto-grants-2010_10
ORD IDord-e2e781d4303b495287866571ae9eea62
Source noteuspto-grants-2010_10