HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → alpha-Hydroxyacetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Benzanilide | HCID 7168 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | HCID 12823444 | HCID 12823444 | — |
| Product | alpha-Hydroxyacetophenone | HCID 68490 | — |
| Product | HCID 4070889 | HCID 4070889 | — |
Reaction Steps
In a third method the 1,2-diphenylquinolones (IV, m = O) are prepared by acylation of an appropriate aniline with an appropriate benzoyl chloride, chlorination of the resulting benzanilide, reaction of the benzimidoyl chloride so obtained with an appropriate 2-hydroxyacetophenone and rearrangement of the resulting 2-acetylphenyl N-phenylbenzimidate. The sequence of reactions is illustrated by the following equations: ##SPC9##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03994902 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-878638959e9b4588b3abc30840a63586 |
| Source note | uspto-grants-1976_11 |