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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551731Generated: November 1, 2026

Phenol → Phenol

https://huagongshe.com/reaction/551731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantTriphenylphosphineHCID 11776—
Reactant2,4-Pentanediol, (-)-HCID 2723683—
Reactant2-methoxyethyl N-(2-methoxyethoxycarbonylimino)carbamateHCID 53384415—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductPhenolHCID 996—
Product(4S,2R)-4-phenoxypentane-2-olHCID 59520617—

Reaction Steps

After phenol (300 mg, 3.19 mmol), triphenylphosphine (1008 mg, 3.83 mmol), (2R,4R)-2,4-pentanediol (399 mg, 3.83 mmol), and THF (12 ml) were added to a 50 ml flask, azodicarboxylic acid bis(2-methoxyethyl) ester (896 mg, 3.83 mmol) dissolved in THF (6 mL) was added dropwise thereto at 20° C., and the reaction was allowed to proceed for 21 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, 40% ethyl acetate-hexane solution) to give (4S,2R)-4-phenoxypentane-2-ol as a colorless oily substance (481 mg, yield: 84%/phenol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947816B2
Source datasetuspto-grants-2011_05
ORD IDord-934670139f494a49892f9eba1b4a2bf0
Source noteuspto-grants-2011_05