HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 2,6-Bis(benzylidene)cyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,6-Bis(benzylidene)cyclohexanone | HCID 95336 | — |
Reaction Steps
To a 0.67 M solution of the benzaldehyde (20.0 mmol) and cyclohexanone (10.0 mmol) in ethanol (15 ml) is added 10 ml 40% KOH at 10° C. After stirring for 12-24 hr at room temperature, the solution is diluted and filtered. The precipitate is recrystallized from ethanol to afford 2,6-dibenzalcyclohexanone and its derivatives. VIII. 2,6-DIBENZYLIDENECYCLOPENTANONE Derivatives
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06906105B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-bf7d0c83c28647ee8d82a3945f26498d |
| Source note | uspto-grants-2005_06 |