HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Butyl bromide → N-butyl-N-acetyl-2,4-difluoroaniline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Butyl bromide | HCID 8002 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Acetamide, N-(2,4-difluorophenyl)- | HCID 96093 | — |
| Katalysator | Benzyl triethylammonium chloride | HCID 66133 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | N-butyl-N-acetyl-2,4-difluoroaniline | HCID 19827549 | 68,7% |
Reaktionsschritte
0.9 g of triethylbenzylammonium chloride, 6.9 g of butyl bromide and a solution of 5.7 g of KOH in 6 ml of water are added to a stirred solution of 3.4 g of N-acetyl-2,4-difluoroaniline (Example 2) in 60 ml of toluene. The emulsion produced is warmed at 97° (reflux). After 1 h, the emulsion is cooled to room temperature and diluted with 20 ml of water. The two phases are separated, and the organic phase is dried over MgSO4 and evaporated in vacuo. The liquid crude product is purified by medium-pressure chromatography. 3.1 g of N-butyl-N-acetyl-2,4-difluoroaniline are obtained as a brownish oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05026625 |
| Quelldatensatz | uspto-grants-1991_06 |
| ORD ID | ord-97ddca6efec049b8af0e4bcb966496bc |
| Quellennotiz | uspto-grants-1991_06 |