HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → Triphenylphosphane dichloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Triphenylphosphine Oxide | HCID 13097 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | Triphenylphosphane dichloride | HCID 13797396 | 200% |
Reaction Steps
In Example 1, 3.36 g (12 millimoles) of triphenylphosphine oxide and 1.54 g (12 millimoles) of oxalyl chloride were dissolved in 50 ml of monochlorobenzene, and the solution was left standing until the evolution of carbon monoxide and carbon dioxide from the solution was completed. A solution of 12 millimoles of triphenylphosphine dichloride in 50 ml of monochlorobenzene was obtained. That is, the conversion of triphenylphosphine oxide to triphenylphosphine dichloride was effected stoichiometrically.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04301301 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-85e2e41d84d5448dbd7d0bf27f7e2d13 |
| Source note | uspto-grants-1981_11 |