HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetate → alpha-Hydroxyacetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetate | HCID 175 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | alpha-Hydroxyacetophenone | HCID 68490 | 64.9% |
Reaction Steps
To a solution of 755 mg of the thus-obtained acetate in nitrobenzene were added 456 mg of finely divided AlCl3, and the mixture was heated for one hour at 120°-125° C. The reaction mixture was diluted by water and extracted with ethyl acetate. The extracted solution was washed with water, sodium hydrogencarbonate solution, water, and saturated saline solution in series and dried over MgSO4. The distillation of the solvent and purification by chromatography through silica gel column gave 490 mg (yield: 64.9%) of the 2-hydroxyacetophenone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04831052 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-b4c147ce093a4fb3bc82a84f9e780656 |
| Source note | uspto-grants-1989_05 |