HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2,6-Dichlorophenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,2,6,6-Tetrachlorocyclohexan-1-one | HCID 77407 | — |
| Product | 2,6-Dichlorophenol | HCID 6899 | 84.4% |
Reaction Steps
236 g (1 mol) of 2,2,6,6-tetrachlorocyclohexanone and 2.5 g (0.01 mol) of triphenylphosphine were introduced into a reactor equipped with a stirrer and a condenser. The mixture was heated at 150°-180° C. under stirring; the reaction was terminated when the evolution of hydrogen chloride from the reaction mixture ceased. The reaction mixture was then distilled under reduced pressure (boiling point (20 mm Hg)=100° C.) to yield 137.5 g of 2,6-dichlorophenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04351969 |
| Source dataset | uspto-grants-1982_09 |
| ORD ID | ord-4a9a90e0a4834ef0983f0689515dbf6d |
| Source note | uspto-grants-1982_09 |