HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → Diphenyl carbonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Product | Diphenyl carbonate | HCID 7597 | — |
Reaction Steps
Example 1 was repeated with 14.1 g of a powdered ditungsten boride from Strem at 140° C. After 2 hours' reaction time, phenol conversion was 8.8%, wherein 4.7 g of phenyl chloroformate and 10.7 g of diphenyl carbonate were formed. Selectivity for carbonates was approximately 98%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05679825 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-350f5d7b365c4d68b9621222e922d310 |
| Source note | uspto-grants-1997_10 |