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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551733Generated: October 26, 2026

Benzoic Acid → (+)-2-Octanol

https://huagongshe.com/reaction/551733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantTriphenylphosphineHCID 11776—
Reactant(+)-2-OctanolHCID 2723888—
Reactant2-methoxyethyl N-(2-methoxyethoxycarbonylimino)carbamateHCID 53384415—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(+)-2-OctanolHCID 2723888—
Product(R)-2-benzoyloxyoctaneHCID 11424832—

Reaction Steps

After (S)-2-octanol (300 mg, 2.30 mmol), triphenylphosphine (725 mg, 2.76 mmol), benzoic acid (338 mg, 2.76 mmol), and THF (12 ml) were added to a 50 ml flask, azodicarboxylic acid bis(2-methoxyethyl) ester (649 mg, 2.76 mmol) dissolved in THF (6 ml) was added dropwise thereto at 20° C., and the reaction was allowed to proceed for two 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, 10% ethyl acetate-hexane solution) to give (R)-2-benzoyloxyoctane as a colorless liquid substance (490 mg, yield: 91%/(S)-2-octanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947816B2
Source datasetuspto-grants-2011_05
ORD IDord-09f26ad9a6ad449092cbb4b556e4323c
Source noteuspto-grants-2011_05