HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → 4-(Diphenylamino)benzaldehyde N-(2,3-Epoxypropyl)-N-Phenylhydrazone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Benzaldehyde, 4-(diphenylamino)- | HCID 77846 | — |
| Product | 4-(Diphenylamino)benzaldehyde N-(2,3-Epoxypropyl)-N-Phenylhydrazone | HCID 85434700 | — |
Reaction Steps
A mixture of phenylhydrazine (0.1 mole, from Aldrich, Milwaukee, Wis.) and 4-(diphenylamino)benzaldehyde (0.1 mole, from Fluka, Buchs SG, Switzerland) was dissolved in 100 ml of isopropanol in a 250 ml 3-neck round bottom flask equipped with a reflux condenser and a mechanical stirrer. The solution was refluxed for 2 hours. At the end of the reaction, as indicated by thin layer chromatography the disappearance of the starting materials, the mixture was cooled to room temperature. The 4-(diphenylamino)benzaldehyde phenylhydrazone crystals that formed upon standing were filtered off, washed with isopropanol, and dried in a vacuum oven at 50° C. for 6 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07326506B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-26673b0a1243455d93a0c710bad81946 |
| Source note | uspto-grants-2008_02 |