Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Reactant | Diglyme | HCID 8150 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Cobalt diacetate | HCID 6277 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Product | Diphenyl carbonate | HCID 7597 | 11.41% |
Reaction Steps
There is introduced into an autoclave, 35.0 g (0.372 mol) of phenol, 1.14 g (3.54 mmol) of TBAB, 0.028 g (0.125 mmol) of Pd(OA)2, 0.018 g (0.102 mmol) of Co(OAc)2, 2.00 g (19.97 mmol) methyl isobutyl ketone (MIBK) and 35 g (261 mmol) of 2-methoxyethyl ether (diglyme). The reactor is sealed, charged with 900 psi CO2, leak-checked, and then exhausted to atmospheric pressure. The reactor is flushed 2×1500 psi CO followed by pressurization to 2100 psi with CO (high pressure leak test) before exhausting the reactor back to atmosphere pressure. The reactor is flushed with 4×1500 psi of O2 and at the end of the fourth oxygen purge cycle, the oxygen atmosphere in the reactor is reduced to 300 psig. There is added to the oxygen atmosphere, 400 psi of CO2 and 900 psi of CO. The reactor is heated to 100° C. Aliquots of the mixture are taken at predetermined times to determine the amount of diphenyl carbonate which has been produced. After each sampling, the reactor atmosphere is rejuvenated by exhausting the atmosphere to 1000 psi (Pt) followed by the addition of 200 psi of oxygen and 700 psi of carbon monoxide. After 5 hours of reaction there is obtained an 11.41% yield of a red-brown diphenyl carbonate. The reaction solution is distilled at 95-110° C. at 15 torr to effect the removal of phenol. The residue is then distilled at 155-165° C. at 15 torr to effect the recovery of diphenyl carbonate. There is obtained 6-10% yield of substantially white diphenyl carbonate. Following the procedure of example 1, active metallic catalyst values are recovered from the distillate residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05142086 |
|---|
| Source dataset | uspto-grants-1992_08 |
|---|
| ORD ID | ord-5afcae1ba1ce47ee9416338876321ffe |
|---|
| Source note | uspto-grants-1992_08 |
|---|