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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyl AcetateHCID 7904—
Reactant4-Hydroxy-2-(3-benzyloxybenzyl)cyclopent-2-enoneHCID 71170034—
SolventMethyl Isobutyl KetoneHCID 7909—
Product(R)-3-(3-benzyloxybenzyl)-4-oxocyclopent-2-enyl acetateHCID 7117004238%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350090B1
Source datasetuspto-grants-2013_01
ORD IDord-d8200ca31ac44ed3ab947ce1f051ac85
Source noteuspto-grants-2013_01