HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701093Generated: October 31, 2026
1,2-Dichloroethane → Triphenylphosphine Oxide
https://huagongshe.com/reaction/1701093
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Catalyst | Cobalt | HCID 104730 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Triphenylphosphine Oxide | HCID 13097 | — |
Reaction Steps
81.7 mg. (0.164 mmol) of cobalt (saloph) pyridine nitro complex and 187 mg. (0.713 mmol) of triphenylphosphine were dissolved in 20 ml. of 1,2-dichloroethane together with 0.5 ml. of pyridine. (The saloph ligand is the tetradentate ligand [1,2-(ortho-OC6H4CH=N)2C6H4 ]2- obtained by condensation reaction of o-diaminobenzene with salicylaldehyde). The resulting solution was stirred under an oxygen atmosphere for 18 hours at 60° C. The resulting reaction product was analyzed by infrared spectroscopy showing a quantitative yield of triphenylphosphine oxide, i.e. 0.713 mmol. This example is illustrative of catalytic oxidation by a cobalt nitro complex having a tetradentate ligand and a monodentate basic ligand in accordance with this invention.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04191696 |
|---|
| Source dataset | uspto-grants-1980_03 |
|---|
| ORD ID | ord-1110662407a24155976d1ff3f5d5c66f |
|---|
| Source note | uspto-grants-1980_03 |
|---|