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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7851Generated: October 26, 2026

1-Penten-3-one → 2-Butyl-5-methoxy-4-methyl-2-(3-oxopentyl)-1-indanone

https://huagongshe.com/reaction/7851

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Penten-3-oneHCID 15394—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-Butyl-5-methoxy-4-methyl-1-indanoneHCID 21990883—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-Butyl-5-methoxy-4-methyl-2-(3-oxopentyl)-1-indanoneHCID 21990930—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 2-butyl-5-methoxy-4-methyl-1-indanone (100 mg, 0.43 mmol) in tetrahydrofuran (0.43 mL) was treated with ethyl vinyl ketone (EVK, 0.064 mL, 0.646 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU, 0.013 mL, 0.086 mmol). The resulting solution was stirred under a nitrogen atmosphere and heated in an oil bath at 60° C. After 24 hour, more EVK (0.064 mL) and DBU (0.013 mL) were added and the solution was heated an additional 24 hours at 60° C. The reaction mixture was diluted with EtOAc (10 mL) and washed with water (10 mL) containing 2N HCl (1 mL). The organic phase was washed with brine (5 mL), dried over MgSO4, filtered, and evaporated under vacuum to provide crude 2-butyl-5-methoxy-4-methyl-2-(3-oxopentyl)-1-indanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087599B2
Source datasetuspto-grants-2006_08
ORD IDord-ab9cbb76965644d483935f81bfcf3531
Source noteuspto-grants-2006_08