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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849365Generated: October 30, 2026

Vinyl Acetate → (2R,3S)-2-acetoxy-3-(4-phenoxyphenyl)-5-phenylpentane

https://huagongshe.com/reaction/849365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyl AcetateHCID 7904—
ReactantTriethylamineHCID 8471—
Reactant(2RS,3SR)-3-(4-phenoxyphenyl)-5-phenylpentan-2-olHCID 19591495—
Product(2R,3S)-2-acetoxy-3-(4-phenoxyphenyl)-5-phenylpentaneHCID 57004388—

Reaction Conditions

Temperature30 °C

Reaction Steps

47.2 g of (2RS,3SR)-3-(4-phenoxyphenyl)-5-phenylpentan-2-ol was dissolved in 470 ml of vinyl acetate, and 19.4 ml of triethylamine was added. Then, 4.7 g of immobilized lipase (Toyothium LIP) was added, followed by stirring at 30° C. for 2 days. The enzyme was filtered off and then, washed with ethyl acetate. The filtrate and the washing liquid were put together, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1→5/1) to obtain 23.8 g of (2R,3S)-2-acetoxy-3-(4-phenoxyphenyl)-5-phenylpentane and 22.2 g of the above identified compound, respectively, as colorless oily substances. Further, the absolute configuration of the above-identified compound was determined by Mosher method (J. Am. Chem. Soc., vol. 113, p. 4092 (1991)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06011174
Source datasetuspto-grants-2000_01
ORD IDord-5962060bad7c45b8a6a5acb63badc035
Source noteuspto-grants-2000_01