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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7831Generated: October 25, 2026

Butanal → 2-Butyl-5-methoxy-1-indanone

https://huagongshe.com/reaction/7831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanalHCID 261—
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant5-Methoxyindan-1-oneHCID 78787—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-Butyl-5-methoxy-1-indanoneHCID 1204575253.2%

Reaction Steps

A mixture of 5-methoxy-1-indanone (25.0 g, 154 mmol), 85% KOH (2.03 g, 30.8 mmol), 10% palladium on activated carbon (2 g), and ethanol (150 mL) was placed under a hydrogen atmosphere and stirred while butyraldehyde (16.7 mL, 185 mmol) was added over 2 minutes. The mixture warmed during the addition. The resulting mixture was hydrogenated at room temperature for 3 hours, then filtered to remove the catalyst. The filtrate was acidified with 2N HCl (15.4 mL, 30.8 mmol) and evaporated under vacuum. The residue was partitioned between EtOAc (500 mL) and water (500 mL). The organic phase was washed with water (500 mL) and brine (100 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (33.5 g). The crude product was purified by column chromatography on EM silica gel 60 (230-400 mesh, 670 g), eluting first with CH2Cl2 and then with 5% EtOAc in CH2Cl2, to afford 2-butyl-5-methoxy-1-indanone (17.9 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087599B2
Source datasetuspto-grants-2006_08
ORD IDord-81064133f67440459d71cf2f2f14c79e
Source noteuspto-grants-2006_08