HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acetic Acid → Benzenamine, 4-chloro-N-ethyl-2-nitro-
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Acetaldehyde | HCID 177 | — |
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | 4-Chloro-2-nitroaniline | HCID 6979 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Ethyl acetate hexane | HCID 21226206 | — |
| Produkt | Benzenamine, 4-chloro-N-ethyl-2-nitro- | HCID 97006 | 50% |
Reaktionsschritte
4-chloro-2-nitroaniline (8.6 g; 0.05 mole), acetaldehyde (5.5 ml; 0.05 mole) and HOAc (4.0 ml; 0.1 moles) were dissolved in toluene (100 ml) and stirred for 1 hr. BH3 * pyridine (5.0 ml; 0.01 moles) was added in 1.0 ml increments. The reaction was exothermic, and the reaction progress was monitored by tlc (40%EtOAc/Hexane). Additional TFA, BH3 * pyridine and acetaldehyde were added until the tlc indicated that the 4-chloro-2-nitroaniline was consumed. The reaction mixture was washed 2X with water and placed on a bed of silica and eluted with 20% EtOAc/Hexane. The product was the first major component to elute. The product was crystallized from MeOH which produced 5.0 g (50%) of a yellow crystalline solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05521193 |
| Quelldatensatz | uspto-grants-1996_05 |
| ORD ID | ord-730cd785fd4d49a6a6507551a1e20aeb |
| Quellennotiz | uspto-grants-1996_05 |