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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045041Generated: October 30, 2026

4-Phenyl-3-Buten-2-one → Benzyl acetone

https://huagongshe.com/reaction/1045041

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenyl-3-Buten-2-oneHCID 15909—
ReactantHCID 178418361HCID 178418361—
SolventMethanolHCID 887—
ProductBenzyl acetoneHCID 17355100.5%

Reaction Steps

Activated Ni EnCat (0.26 g, water wet, 20 mol % Ni on substrate) was washed with MeOH three times to remove water and added to benzalacetone (0.148 g, 1 mmol) dissolved in MeOH (4 ml) in a pressure vessel. The vessel was sealed and purged twice with hydrogen then pressurised to 5-6 bar with hydrogen and the contents magnetically stirred at room temperature. Progress of reaction was carried out by GCMS analysis. After 24 h the hydrogen was vented and the Ni EnCat beads removed by filtration. The filtrate was concentrated on a rotary evaporator to give 4-phenylbutanone (0.149 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563753B2
Source datasetuspto-grants-2013_10
ORD IDord-231242dbf25c4f559cd3b1d8a730d25e
Source noteuspto-grants-2013_10