HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroquinone → Diphenyl carbonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | HCID 21441352 | HCID 21441352 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | Tetraphenylphosphonium Bromide | HCID 2724163 | — |
| Product | Diphenyl carbonate | HCID 7597 | 23.7% |
Reaction Steps
The same operation as that in Example 1 was performed using 3.1 g (33 mmol) of phenol, 25.5 mg (0.012 mmol Pd) of 5%-palladium/carbon, 4.0 mg (0.012 mmol) of cerium (III) acetate monohydrate, 101 mg (0.24 mmol) of tetraphenylphosphonium bromide and 13 mg (0.12 mmol) of hydroquinone. After reaction for 3 hours, diphenyl carbonate was obtained with a yield of 23.7% (3.9 mmol). Phenyl salicylate and p-phenoxyphenol were produced as by-products with yields of 0.55% (0.090 mmol) and 0.15% (0.025 mmol), respectively. The selectivity of p-phenoxyphenol was 0.6%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05543547 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-11ede1b21198470cba4791639194e7f5 |
| Source note | uspto-grants-1996_08 |