HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803635Generated: November 1, 2026
Acetic Acid → (R)-3-(3-methoxybenzyl)-4-oxocyclopent-2-enyl acetate
https://huagongshe.com/reaction/1803635
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Vinyl Acetate | HCID 7904 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | 4-Hydroxy-2-(3-methoxybenzyl)cyclopent-2-enone | HCID 71170038 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | (R)-3-(3-methoxybenzyl)-4-oxocyclopent-2-enyl acetate | HCID 71170032 | 93% |
Reaction Steps
4-Hydroxy-2-(3-methoxybenzyl)cyclopent-2-enone (9 g, 41.26 mmol) was dissolved in isobutyl methyl ketone (90 mL), and vinyl acetate (8.4 g, 97.57 mmol) and Lipase derived from Pseudomonas cepacia (0.9 g) were added to the solution, and the mixture was stirred at room temperature overnight. The reaction mixture was filtered to remove the Lipase and the filtrate was evaporated. The resulting residue was dissolved in PhCH3 (150 ml), and triphenylphosphine (6.5 g; 24.78 mmol) and AcOH (1.61 g, 26.81 mmol) were added to the solution. Then diisopropylazodicarboxylate (5 g, 24.72 mmol) was added to the mixture at 5° C. After the reaction was completed, the reaction mixture was filtered to remove the precipitate and the filtrate was evaporated. The residue was purified by chromatography on a silica gel column using hexane-EtOAc as eluent to give the (R)-3-(3-methoxybenzyl)-4-oxocyclopent-2-enyl acetate as yellow oil: 10 g (yield: 93%, 95% ee by HPLC using a chiral column)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08350090B1 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-b5d27e2556a84897bdcb1111261a2766 |
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| Source note | uspto-grants-2013_01 |
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