HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methylcyclopentanone → 2-Methyl-5-(4-methoxybenzylidene)-cyclopentanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methylcyclopentanone | HCID 14265 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methyl-5-(4-methoxybenzylidene)-cyclopentanone | HCID 53764538 | 94% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
A solution of 2.8 g of 85% strength aqueous potassium hydroxide solution and 250 ml of water was charged to a 0.71 stainless-steel autoclave, and 49 g of 2-methylcyclopentanone and 68 g of p-anisaldehyde were added. The mixture was subsequently heated to 120° C. with stirring under the intrinsic pressure and subsequently stirred under the intrinsic pressure (1.5 bar) for 3 hours. After cooling to room temperature, the precipitated solid was filtered off with suction, washed to neutrality with water and dried in a vacuum oven at 55° C. In this way 101.5 g of 2-methyl-5-(4-methoxybenzylidene)-cyclopentanone (pure according to gas chromatography) were obtained. This corresponds to a yield of 94% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05741937 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-4c4f2382d18e480a945be9e56757d5b1 |
| Source note | uspto-grants-1998_04 |