HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Ethanone, 2-(acetyloxy)-1-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Chloroacetophenone | HCID 10757 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethanone, 2-(acetyloxy)-1-phenyl- | HCID 222851 | 79.4% |
Reaction Steps
78.5 g (0.80 mol) of potassium acetate, 5.0 g (0.08 mol) of acetic acid and 123.7 g (0.80 mol) of 2-chloroacetophenone was heated under reflux in 500 ml of ethanol for 6 hours. After the completion of heating, the reaction solution was cooled to room temperature, precipitated potassium chloride was filtered off, and ethanol was evaporated off under reduced pressure, giving an oily and caramel-like substance. The obtained oily substance was poured into 1 liter of water and the precipitated yellowish-brown crystalline solid was filtered off, followed by recrystallization from methanol, giving 113.1 g (0.635 mol, 79.3% yield) 2-acetoxyacetophenone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07661577B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-786a30af639e40e387f335d03bd3d6ad |
| Source note | uspto-grants-2010_02 |