HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetoxyacetyl chloride → 2-(Acetoxyacetylamino)-6-nitrobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetoxyacetyl chloride | HCID 26297 | — |
| Reactant | 2-Amino-6-nitrobenzonitrile | HCID 12715729 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-(Acetoxyacetylamino)-6-nitrobenzonitrile | HCID 14986282 | — |
Reaction Steps
A solution of 2-amino-6-nitrobenzonitrile (6.5 g) in pyridine (100 ml) is cooled in an ice bath and thereto is added dropwise acetoxyacetyl chloride (4.4 ml). The mixture is stirred at room temperature for 1 hour, and thereafter, pyridine is distilled off under reduced pressure, and then water is added thereto, and the mixture is extracted with methylene chloride. The organic layer is washed with 1N hydrochloric acid and dried over anhydrous sodium sulfate, and the solvent is distilled off under reduced pressure. The resulting crude crystals are recrystallized from ethanol to give the title compound (5.8 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-6c0f96e5dae34bae80d214d5299054b8 |
| Source note | uspto-grants-1991_08 |