HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → Ethanone, 1-(4-octylphenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Octylbenzene | HCID 16607 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | Ethanone, 1-(4-octylphenyl)- | HCID 66344 | — |
Reaction Steps
Aluminum chloride (22.6 g) is suspended in dichloroethane (500 ml) and octylbenzene (16) (21.5 g) is added at room temperature. To the mixture is added acetyl chloride (8.87 g) under ice-cooling. The mixture is stirred at room temperature overnight. The reaction mixture is poured into ice water and extracted with ether. The organic layer is washed with brine and dried over sodium sulfate. The solvent is evaporated to give 4′-octylacetophenone (18′) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06605744B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-f0335febdb6e4fc9a41e2e6dafd45797 |
| Source note | uspto-grants-2003_08 |