Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Phenyl-1,4-pentanedione | HCID 136371 | 40% |
Reaction Steps
To 1200 ml of dimethylformamide (DMF) containing 3 moles of benzaldehyde and heated at 35° C., a mixed solution of 0.3 mole of sodium cyanide and 2400 ml of DMF was added dropwise in 30 minutes, and the reaction was carried out for further 30 minutes with stirring. To the reaction solution, a mixed solution of 2.25 moles of methyl vinyl ketone and 2400 ml of DMF was added dropwise in 30 minutes, and the reaction was carried out for further 1 hour. After the reaction, water was poured into the reaction solution, followed by extraction with chloroform. The obtained chloroform solution was washed with dilute sulfuric acid, saturated aqueous solution of sodium bicarbonate, and water in this order, and dried over anhydrous sodium sulfate. The solvent was removed by distillation. The resulting residue was distilled under reduced pressure to give a fraction of pale yellow liquid of 1-phenyl-1,4-pentanedione having a boiling point of 124°-127° C./0.15 mmHg (yield 40% ).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05359085 |
|---|
| Source dataset | uspto-grants-1994_10 |
|---|
| ORD ID | ord-9eb1c49f4f0f42ccb0ccd4e6859312a1 |
|---|
| Source note | uspto-grants-1994_10 |
|---|