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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551732Generated: October 27, 2026

Phenol → Phenol

https://huagongshe.com/reaction/551732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantTriphenylphosphineHCID 11776—
Reactant2,4-Pentanediol, (-)-HCID 2723683—
ReactantDIAD tolueneHCID 66880968—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductPhenolHCID 996—
Product(4S,2R)-4-phenoxypentane-2-olHCID 59520617—

Reaction Steps

After phenol (300 mg, 3.19 mmol), triphenylphosphine (1006 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, a 40% azodicarboxylic acid diisopropyl ester-toluene solution (2.01 ml, 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 (461 mg, yield: 80%/phenol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947816B2
Source datasetuspto-grants-2011_05
ORD IDord-625a0b6ff44d49129e9aa064a63785c0
Source noteuspto-grants-2011_05