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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372494Generated: November 1, 2026

Butanal → HCID 17972753, compound

https://huagongshe.com/reaction/1372494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanalHCID 261—
ReactantPotassium HydroxideHCID 14797—
ReactantN-(1-Oxo-2,3-dihydro-1H-inden-5-yl)acetamideHCID 312894—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 17972753HCID 1797275369%

Reaction Steps

5-(Acetylamino)-1-indanone (10.0 g, 52.3 mmol) was added to a solution of KOH (87.7%, 0.66 g, 10.3 mmol) in EtOH (200 mL). The resulting suspension was stirred at room temperature while butyraldehyde (6.1 mL, 67.8 mmol) was added dropwise over two minutes. After stirring at room temperature for an additional 15 minutes, the mixture was treated with 10% Pd/C and stirred under a H2 atmosphere (balloon) for 19 hours. The mixture was filtered through a pad of silica gel and the pad washed with EtOAc. The filtrate was washed with 1N HCl, 5% NaHCO3, water, and brine, dried over MgSO4, filtered, and concentrated under vacuum to an orange oil (12 g). The crude product was purified by Biotage flash chromatography on a 75 L silica gel column (7.5×35 cm), eluting with 2:1 hexane-EtOAc, to afford 5-(acetylamino)-2-butyl-1-indanone (8.8 g, 69%) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157604B2
Source datasetuspto-grants-2007_01
ORD IDord-ae3ff0003c904ecc866f1313808507f0
Source noteuspto-grants-2007_01