HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenyl-3-Buten-2-one → Benzyl acetone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenyl-3-Buten-2-one | HCID 15909 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Benzyl acetone | HCID 17355 | 100.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08563753B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-231242dbf25c4f559cd3b1d8a730d25e |
| Source note | uspto-grants-2013_10 |