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 | Tetrabutylammonium Bromide | HCID 74236 | — |
| Product | Diphenyl carbonate | HCID 7597 | 12.6% |
Reaction Steps
The same operation as that in Example 1 was performed using 4.5 g (49 mmol) of phenol, 12.7 mg (0.006 mmol Pd) of 5%-palladium/carbon, 2.0 mg (0.006 mmol) of cerium (III) acetate monohydrate, 127 mg (0.40 mmol) of tetra-n-butylammonium bromide and 21 mg (0.19 mmol) of hydroquinone. After reaction for 3 hours, diphenyl carbonate was obtained with a yield of 12.6% (3.0 mmol). Phenyl salicylate and p-phenoxyphenol were produced as by-products with yields of 0.30% (0.073 mmol) and 0.18% (0.044 mmol), respectively. The selectivity of p-phenoxyphenol was 1.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05543547 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-6c5e8de1692b4eafa40a13bc086500a4 |
| Source note | uspto-grants-1996_08 |