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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551727Generated: November 1, 2026

Benzoic Acid → Benzoic Acid

https://huagongshe.com/reaction/551727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantTriphenylphosphineHCID 11776—
Reactant2,4-Pentanediol, (-)-HCID 2723683—
Reactant2-methoxyethyl N-(2-methoxyethoxycarbonylimino)carbamateHCID 53384415—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductBenzoic AcidHCID 243—
Product(4S,2R)-4-benzoyloxypentane-2-olHCID 59520616—

Reaction Steps

After benzoic acid (300 mg, 2.46 mmol), triphenylphosphine (775 mg, 2.95 mmol), (2R,4R)-2,4-pentanediol (308 mg, 2.95 mmol), and THF (12 ml) were added to a 50 ml flask, azodicarboxylic acid bis(2-methoxyethyl) ester (691.1 mg, 2.95 mmol) dissolved in THF (6 mL) was added dropwise thereto at 20° C., and the reaction was allowed to proceed for one hour. 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-benzoyloxypentane-2-ol as a colorless oily substance (379 mg, yield: 74%/benzoic acid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947816B2
Source datasetuspto-grants-2011_05
ORD IDord-0bc04bfffcb4429d8f738eab7ce1af57
Source noteuspto-grants-2011_05