HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-(p-Tolyl)-2-butanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-Carboethoxy-4-(4-methylphenyl)but-3-en-2-one | HCID 367489 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(p-Tolyl)-2-butanone | HCID 5463908 | — |
Reaction Steps
3-Carboethoxy-4-(4-methylphenyl)but-2-one (20 g), (prepared by hydrogenation over PtO2 at 1 atmosphere of 3-carboethoxy-4-(4-methylphenyl)but-3-en-2-one) was heated under reflux for 3.5 h in a mixture of glacial acetic acid (48 ml), concentrated hydrochloric acid (5.6 ml) and water (30 ml). The solvent was evaporated, the residue dissolved in xylene, washed with water, dried and evaporated. The residue was distilled to give 4-(4-methylphenyl)butan-2-one, 11.0 g, bp 80-90/1 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04588749 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-6759616b84334d159ace86c71b43a672 |
| Source note | uspto-grants-1986_05 |