HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → Diphenyl carbonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Catalyst | Titanium oxide (Ti3O) | HCID 162651 | — |
| Product | Diphenyl carbonate | HCID 7597 | 2,036% |
Reaction Steps
In a plane-joint jar with flow spoilers, a gas-dispersion stirrer and reflux condenser, 0.75 mol/h phosgene was continuously bubbled into 141 g (1.50 moles) of phenol at 140° C. in the presence of 14.1 g (10 wt % relative to phenol) of a powdered titanium dioxide from the Riedel de Haen company. After about 2 h reaction time, the phenol conversion was 12.5%, whereby 0.7 g phenyl chloroformate and 19.5 g diphenyl carbonate were formed. The selectivity to carbonate esters was >99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05527942 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-c77c45f7d13644d3954aed53fde719d7 |
| Source note | uspto-grants-1996_06 |