HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-(Acetoxyacetylamino)-6-aminobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | 2-(Acetoxyacetylamino)-6-nitrobenzonitrile | HCID 14986282 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Product | 2-(Acetoxyacetylamino)-6-aminobenzamide | HCID 14986279 | — |
Reaction Steps
To a mixture of 2-(acetoxyacetylamino)-6-nitrobenzonitrile (5.7 g) and ethanol (50 ml) are added cyclohexene (10.5 ml) and 10% palladium-carbon (4.7 g). The mixture is refluxed for 20 minutes, and the reaction mixture is cooled to room temperature, and the solid materials are filtered off. The filtrate is distilled under reduced pressure. The residual crude crystals are recrystallized from ethanol to give the title compound (1.2 g) having the following physical properties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05041462 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-3ea07f62c85c475d8ad9dfedc7d035e2 |
| Source note | uspto-grants-1991_08 |