HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → Benzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Benzhydrol | HCID 7037 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Product | Benzophenone | HCID 3102 | — |
| Product | Acetophenone | HCID 7410 | — |
Reaction Steps
In page 762 of the "Lecture Draft II" (1994) of 67th Spring Annual Meeting of Chemical Society of Japan, it is reported that oxidation of an alcohol such as benzyl alcohol or benzhydrol with air using vanadomolybdophosphoriate and N-hydroxyphthalimide provides a ketone such as acetophenone or benzophenone in a high yield, and that oxidation of tetralin, isochroman or adamantane with oxygen using N-hydroxyphthalimide gives a corresponding monoalcohol or monoketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05958821 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-db5a0bf45da04ce8bdf511cbec50699c |
| Source note | uspto-grants-1999_09 |