HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Phenol, 2-[[(2-hydroxyphenyl)imino]methyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2-Aminophenol | HCID 5801 | — |
| Reactant | 2-Hydroxy-1-naphthaldehyde | HCID 12819 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Phenol, 2-[[(2-hydroxyphenyl)imino]methyl]- | HCID 74479 | — |
Reaction Steps
The preparations of compounds used in this invention are shown in detail below. In general [nBu4N][OsVI(N)Cl4] is reacted with the ligand in a suitable organic solvent, such as methanol, ethanol or dichloromethane. The Schiff base ligands 5-X—H2salpa (salpa=N-salicylidene-2-aminophenol dianions) are synthesized by condensation of the appropriate 2-hydroxybenzyaldehyde with the 2-aminophenol in refluxing ethanol. The Schiff base ligand nalph is synthesized by condensation of the 2-hydroxy-1-naphthaldehyde with the 2-aminophenol in refluxing ethanol. [NnBu4][OsVI(N)Cl4] were prepared by a literature procedure (Griffith, W. P. and Pawson, D. J. J. Chem. Soc., Dalton Trans. 1973, 1315.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383673B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-b9b91f71ceec4cf09f066b0829d25792 |
| Source note | uspto-grants-2013_02 |