Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Mesitylene | HCID 7947 | — |
| Edukt | Sodium Cyanide | HCID 8929 | — |
| Edukt | Butylimidazole | HCID 61347 | — |
| Edukt | 2-amino-5-bromo-N,3-dimethylbenzamide | HCID 44227575 | — |
| Edukt | NaOH NaClO | HCID 86647248 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-Amino-5-cyano-N,3-dimethylbenzamide | HCID 25157282 | — |
Reaktionsschritte
A 500-mL four-necked flask equipped with a mechanical stirrer, thermocouple, condenser, side-arm addition funnel and sodium hydroxide/sodium hypochlorite scrubber was charged with 2-amino-5-bromo-N,3-dimethylbenzamide (prepared by the method of Reference Example 1) (24.6 g, 0.10 mol, 99% purity) and mesitylene (100 g) while maintaining an atmosphere of nitrogen through a gas inlet line connected to the condenser. The reaction mixture was stirred at room temperature and sodium cyanide (ground to a powder just prior to use) (7.7 g, 0.15 mol, assuming 95% purity), copper(I) iodide (2.9 g, 0.015 mol, 98% purity) and 1-butyl-1H-imidazole (10.8 g, 0.085 mol, 98% purity) were added, after which time the nitrogen inlet line was attached directly to the reaction flask. The reaction mixture was heated at reflux (about 166-170° C.) for 7 h, while venting through the scrubber. After cooling overnight, water (100 mL) was added to the reaction mixture and stirring was continued for 1 h. The mixture was filtered, and the solid collected was washed with water (3×50 mL), mesitylene (50 g) and dried to a constant weight in a vacuum-oven at 55° C. to give the title compound as a light yellow solid (16.9 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08242279B2 |
|---|
| Quelldatensatz | uspto-grants-2012_08 |
|---|
| ORD ID | ord-4a332d112e6d42479324f6c5c6123f12 |
|---|
| Quellennotiz | uspto-grants-2012_08 |
|---|