HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → Naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Naphthalene | HCID 931 | — |
| Reactant | Hydrofluoric Acid | HCID 14917 | — |
| Product | Naphthalene | HCID 931 | 48% |
| Product | 1-Naphthol | HCID 7005 | 42.3% |
| Product | 2-Naphthol | HCID 8663 | 0.7% |
Reaction Steps
When carrying out the hydroxylation of naphthalene with a molar excess of H2O2 (90%) in a conventional acid system, such as anhydrous hydrogen fluoride, at temperatures ranging from -10° to 0° C. and at atmospheric or slightly superatmospheric pressure, 42.3% α-naphthol and only 0.7% β-naphthol were obtained, with about 9% of polymeric higher molecular weight product and 48% of naphthalene can be recovered unchanged. The yield of α-naphthol is 81% with an isomeric purity of 98.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04419528 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-50bd0ef1628d45e0bfdafea5a3fffe7b |
| Source note | uspto-grants-1983_12 |