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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Vinyl Acetate | HCID 7904 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (2RS,3SR)-3-(4-phenoxyphenyl)-5-phenylpentan-2-ol | HCID 19591495 | — |
| Product | (2R,3S)-2-acetoxy-3-(4-phenoxyphenyl)-5-phenylpentane | HCID 57004388 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06011174 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-5962060bad7c45b8a6a5acb63badc035 |
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| Source note | uspto-grants-2000_01 |
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