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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566726Generated: October 30, 2026

Acetic Anhydride → 4-Acetoxy-3-pyridine-4-yl-4-m-tolyl-cyclopent-2-en-1-one

https://huagongshe.com/reaction/566726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant4-Hydroxy-3-pyridine-4-yl-4-m-tolyl-cyclopent-2-en-1-oneHCID 21266447—
Reactant4-Hydroxy-4-pyridine-4-yl-3-m-tolyl-cyclopent-2-en-1-oneHCID 21266548—
SolventDichloromethaneHCID 6344—
Product4-Acetoxy-3-pyridine-4-yl-4-m-tolyl-cyclopent-2-en-1-oneHCID 21266556—

Reaction Steps

To a solution of 4-hydroxy-4-pyridine-4-yl-3-m-tolyl-cyclopent-2-en-1-one, and it's regioisomer 4-hydroxy-3-pyridine-4-y1-4-m-toly1-cyclopent-2-en-1-one prepared as described in Example 8, Step E (265 mg, 1.0 mmole) in methylene chloride (5 mL) was added dimethylamino pyridine (183 mg, 1.5 mmole) and acetic anhydride (0.12 mL, 1.2 mmole) at r.t. The reaction mixture was stirred at that temperature for 1 hr before quenching the reaction with 1 mL of methanol. Concentration and purification (silica, hexane/ethyl acetate) gave the title compound as the slower eluting isomer. MS (m/z): Calcd. C19H17NO3(M+): 307, found (M+H) +: 308.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174901B1
Source datasetuspto-grants-2001_01
ORD IDord-8ad9a94d686d46bdb219eae6e7d60c80
Source noteuspto-grants-2001_01