HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzaldehyde → HCID 67897623, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67897623 | HCID 67897623 | — |
Reaction Steps
p-Nitrobenzaldehyde is reacted with acetophenone and sodium hydroxide in ethanol to produce 3-(p-nitrophenyl)-3-hydroxy-1-phenyl propanone. The resulting compound is reacted with KHSO4 to obtain p-nitrochalcone. p-Nitrochalcone is hydrogenated in the presence of platinum catalyst to produce 3-(p-aminophenyl)-1-phenyl propanone. The resulting compound is reacted with potassium hydroxide and hydrazine in triethylene glycol to produce p-aminodiophenylpropane. p-Aminodiphenylpropane is reacted with fuming nitric acid and acetic acid anhydride to obtain 1-(p-aminophenyl)-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-6d8e349132af4092a25fed2614f888b7 |
| Source note | uspto-grants-1992_03 |