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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803640Generated: November 1, 2026

Sodium Hydroxide → (R)-4-hydroxy-2-(3-benzyloxybenzyl)cyclopent-2-enone

https://huagongshe.com/reaction/1803640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant(R)-3-(3-benzyloxybenzyl)-4-oxocyclopent-2-enyl acetateHCID 71170042—
SolventPotassium phosphate (KH5(PO4)2)HCID 23690538—
Product(R)-4-hydroxy-2-(3-benzyloxybenzyl)cyclopent-2-enoneHCID 7117004783%

Reaction Steps

(R)-3-(3-Benzyloxybenzyl)-4-oxocyclopent-2-enyl acetate (1.8 kg, 5.35 mol) was added to KH2PO4—H3PO4 buffer solution (20 L). The mixture was added Lipase derived from Pseudomonas cepacia and 1N NaOH was slowly added to the solution at room temperature to keep the ph=7˜7.5. After 8 hours, (R)-3-(3-Benzyloxybenzyl)-4-oxocycl opent-2-enyl acetate remained about 10%, The reaction mixture was filtered to remove Lipase and the filtrate was extracted with EtOAc, dried over MgSO4, and evaporated. The resulting residue was purified by chromatography on a silica gel column using hexane-EtOAc as eluent to give the (R)-4-hydroxy-2-(3-benzyloxybenzyl)cyclopent-2-enone as yellow oil: 1.3 kg (yield: 83%, >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-0fc6d7a88086431f91364095d38e1986
Source noteuspto-grants-2013_01