HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cinnamoylbenzene → 2-(3-oxo-1,3-diphenylpropyl)cyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cinnamoylbenzene | HCID 7189 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(3-oxo-1,3-diphenylpropyl)cyclohexanone | HCID 272856 | — |
Reaction Steps
Ten parts of benzalacetophenone and 5 parts of cyclohexanone was dissolved in 200 mL of ethyl alcohol and a solution of 5 parts of sodium hydroxide in 100 ml of ethanol was added to the reaction mixture. After 30 minutes the solution became cloudy and white solid was appeared. The reaction mixture was stirred for 10 hours at room temperature and solid was filtered, washed with water and then with 100 ml of ethyl alcohol. The white solid was dried under reduced pressure,with a yield of 12 parts. The reaction proceeded as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06461876B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-872992daec6c4da09d88e3046d8c3c3d |
| Source note | uspto-grants-2002_10 |