Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 11458200 | HCID 11458200 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Oxo-1-phenylhexan-3-yl acetate | HCID 23466017 | — |
Reaction Steps
To a solution of 850 mg of 4-hydroxy-6-phenylhexan-2-one (T. Mukaiyama et al., Chemistry Letters 1976, 95) in 10 ml of methylene chloride were added 1 ml of acetic anhydride and 0.8 ml of pyridine under ice-cooling at 0° C., and then stirring was continued for further 1 hr at room temperature. The reaction mixture was poured into water, the methylene chloride layer was washed with water, dried over anhydrous sodium sulfate, and the solvent was evaporated to afford 1.10 g of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04262013 |
|---|
| Source dataset | uspto-grants-1981_04 |
|---|
| ORD ID | ord-3af3535ac29b46e584147b8beb213a33 |
|---|
| Source note | uspto-grants-1981_04 |
|---|