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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803639Generated: October 30, 2026

Acetic Acid → (R)-3-(3-benzyloxybenzyl)-4-oxocyclopent-2-enyl acetate

https://huagongshe.com/reaction/1803639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantVinyl AcetateHCID 7904—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant4-Hydroxy-2-(3-benzyloxybenzyl)cyclopent-2-enoneHCID 71170034—
SolventMethyl Isobutyl KetoneHCID 7909—
Product(R)-3-(3-benzyloxybenzyl)-4-oxocyclopent-2-enyl acetateHCID 7117004275%

Reaction Steps

4-Hydroxy-2-(3-Benzyloxybenzyl)cyclopent-2-enone (2.1 kg, 7.14 mol) was dissolved in isobutyl methyl ketone (21 L), and vinyl acetate (4.2 kg, 51.16 mol) and Lipase derived from Pseudomonas cepacia (210 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 dissolved in PhCH3 (20 L), and triphenylphosphine (625 g, 2.38 mol) and AcOH (145 g, 2.41 mol) was added to the solution. Then diisopropylazodicarboxylate (413 g, 2.04 mol) 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 dissolved in EtOAc (5 L) and hexane (5 L) was added. The mixture was stirred at room t temperature overnight. The 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-benzyloxybenzyl)-4-oxocyclopent-2-enyl acetate as yellow oil: 1.8 kg (yield: 75%, 97% ee by HPLC using a chiral column)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350090B1
Source datasetuspto-grants-2013_01
ORD IDord-1cc81f4ae47e40b38c84fb689e757f01
Source noteuspto-grants-2013_01