HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 21320435, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Piperonal | HCID 8438 | — |
| Reactant | (4-Aminophenoxy)benzene | HCID 8764 | — |
| Reactant | 54758-86-0 | HCID 4381618 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 21320435 | HCID 21320435 | — |
Reaction Steps
The starting material used for catalytic hydrogenation, 4-phenoxy-(3,4-methylenedioxy-benzylidene)-aniline, is prepared as follows: the solution of 75 g of 3,4-methylenedioxy-benzaldehyde (piperonal) and 92.5 g of 4-aminodiphenyl ether in 500 ml of benzene is refluxed, with separation of water, for 8 hours. After the water has been completely separated, the reaction mixture is concentrated by evaporation; the crystals precipitated after cooling to about +5° C. are filtered off under suction; the crystal mass is recrystallised firstly in anhydrous benzene and subsequently in acetonitrile to thus obtain pure 4-phenoxy-(3,4-methylenedioxybenzylidene)-aniline, M.P. 89°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04153731 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-0e55f168d09742e0afd15b8d3447178d |
| Source note | uspto-grants-1979_05 |