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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803636Generated: November 2, 2026

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

https://huagongshe.com/reaction/1803636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPotassium phosphate (KH5(PO4)2)HCID 23690538—
Reactant(R)-3-(3-methoxybenzyl)-4-oxocyclopent-2-enyl acetateHCID 71170032—
Product(R)-4-hydroxy-2-(3-methoxybenzyl)cyclopent-2-enoneHCID 7117005770%

Reaction Steps

(R)-3-(3-Methoxybenzyl)-4-oxocyclopent-2-enyl acetate (0.1 g, 0.38 mmol) was added to KH2PO4—H3PO4 buffer (1 ml). The mixture was added thereto 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 3 hours, about 10% of (R)-3-(3-methoxybenzyl)-4-oxocyclopent-2-enyl acetate remained. 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-methoxybenzyl)cyclopent-2-enone as yellow oil: 58 mg (yield: 70%, >99.5% ee by HPLC using a chiral column)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350090B1
Source datasetuspto-grants-2013_01
ORD IDord-91de5c71c81e42229c8d3464dcbe0f02
Source noteuspto-grants-2013_01