HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetophenone → Benzonitrile, 4-(3-oxo-3-phenyl-1-propenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Cyanobenzaldehyde | HCID 101209 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 54423443 | HCID 54423443 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Benzonitrile, 4-(3-oxo-3-phenyl-1-propenyl)- | HCID 5367161 | — |
Reaction Steps
1 Mol of cyanobenzaldehyde is reacted with 1 mol of acetophenone and sodium hydroxide in ethanol. The resulting 3-(p-cyanophenyl)-3-phenylpropanone is reacted with KHSO4 to obtain p-cyanochalcone. The p-cyanochalcone is hydrogenated in the presence of a platinum catalyst to produce 3-(p-cyanophenyl)-1-phenylpropanone. The resulting compound is reacted with hydrazine and potassium hydroxide in triethylene glycol to produce p-cyanodiphenylpropane. The p-cyanodiphenylpropane is reacted with fuming nitric acid and acetic acid anhydride to produce 1-(p-cyanophenyl)-3-(p-nitrophenyl)-propane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05101411 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-11cad1fb400f4dff84d70cc150eefec4 |
| Source note | uspto-grants-1992_03 |