HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-Methyl-4-(4-methylphenyl)-1-(3-phenoxyphenyl)pent-1-en-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Phenoxybenzaldehyde | HCID 38284 | — |
| Reactant | 3-Methyl-3-(4-methylphenyl)butan-2-one | HCID 13603223 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Methyl-4-(4-methylphenyl)-1-(3-phenoxyphenyl)pent-1-en-3-one | HCID 54572199 | 97% |
Reaction Steps
To 50 ml of ethanol were added 5.3 g of 2-(4-methylphenyl)-2-methyl-3-butanone, 6.0 g of 3-phenoxybenzaldehyde and 6.0 g of KOH, and the mixture was stirred at room temperature for one hour and 20 minutes. Then, the reaction mixture was poured into 300 ml of water and extracted with benzene. The benzene extract was washed with water and dried, and the solvent was evaporated under reduced pressure to give 10.4 g of crude 1-(3-phenoxyphenyl)-4-(4-methylphenyl)-4-methyl-1-penten-3-one. Then, the crude product was purified by column chromatography on 250 g of silica gel (eluent:benzene) to give 6.8 g of pure 1-(3-phenoxyphenyl)-4-(4-methylphenyl)-4-methyl-1-penten-3-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04661501 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-ec50a8bf83244c6eb6e0c78c25776306 |
| Source note | uspto-grants-1987_04 |