HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Trifluoroacetic anhydride → 4-chloro-2-fluoro-5-methyl-6-nitro-N-phenoxycarbonylaniline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Trifluoroacetic anhydride | HCID 9845 | — |
| Edukt | Ammonium nitrate | HCID 22985 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 4-chloro-2-fluoro-5-methyl-N-phenoxycarbonylaniline | HCID 18615647 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 4-chloro-2-fluoro-5-methyl-6-nitro-N-phenoxycarbonylaniline | HCID 18615646 | 103,1% |
Reaktionsschritte
4-Chloro-2-fluoro-5-methyl-N-phenoxycarbonylaniline (7.1 g, 25.4 mmol) was dissolved in chloroform (68 ml) and trifluoroaceticanhydride (13.5 ml) and ammonium nitrate (2.4 g, 30.5 mmol) were slowly added with stirring at ambient temperature. The stirring was continued for 18 hr when a second batch of ammonium nitrate (0.4 g, 5 mmol) was added and stirring continued for 8 hr. Water was added and solution was neutralized by slow addition of sodium bicarbonate solution followed by extraction with chloroform. Organic layer was dried and evaporated under reduced pressure to afford an oily product (8.5 g) which was used for the next step without purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06355799B1 |
| Quelldatensatz | uspto-grants-2002_03 |
| ORD ID | ord-e79c080beabd48e5a7b746e48164ca14 |
| Quellennotiz | uspto-grants-2002_03 |