HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803638Generated: November 2, 2026
Vinyl Acetate → (R)-3-(3-benzyloxybenzyl)-4-oxocyclopent-2-enyl acetate
https://huagongshe.com/reaction/1803638
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Vinyl Acetate | HCID 7904 | — |
| Reactant | 4-Hydroxy-2-(3-benzyloxybenzyl)cyclopent-2-enone | HCID 71170034 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | (R)-3-(3-benzyloxybenzyl)-4-oxocyclopent-2-enyl acetate | HCID 71170042 | 38% |
Reaction Steps
4-Hydroxy-2-(3-Benzyloxybenzyl)cyclopent-2-enone (5.73 g, 19.48 mmol) was dissolved in isobutyl methyl ketone (60 mL), and vinyl acetate (11.2 g, 13.01 mmol) and Lipase derived from Alculigenese spp (0.6 g) was added to the solution, and the mixture was stirred at room temperature for 1 day. The reaction mixture was filtered to remove Lipase and the filtrate was evaporated. The resulting residue was purified by chromatography on a silica gel column using hexane-EtOAc as eluent to give the (R)-3-(3-benzyloxybenzyl)-4-oxocyclopent-2-enyl acetate as yellow oil: 2.51 g (yield: 38%, 96% ee by HPLC using a chiral column) and (S)-4-hydroxy-2-(3-(benzyloxy)benzyl)cyclopent-2-enone as yellow oil: 2.68 g (yield: 47%, >99% ee by HPLC using a chiral column)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08350090B1 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-d8200ca31ac44ed3ab947ce1f051ac85 |
|---|
| Source note | uspto-grants-2013_01 |
|---|