HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
O-Toluidine → N-Benzyl-o-toluidine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | O-Toluidine | HCID 7242 | — |
| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | N-Benzyl-o-toluidine | HCID 79402 | 43,2% |
Reaktionsschritte
To a solution of 2-methylaniline (1.0 g) and triethylamine (0.95 g) in N,N-dimethylformamide (15 ml) was added benzyl bromide (1.9 g) at ambient temperature and the mixture was stirred at ambient temperature overnight. The reaction mixture was diluted with ethyl acetate and it was washed with water and brine. Drying, filtering and the removal of solvents afforded a crude product. The crude product was chromatographed on silica gel (n-hexane:ethyl acetate=10:1) to give N-benzyl-2-methylaniline (795 mg) as a slightly yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06211242B1 |
| Quelldatensatz | uspto-grants-2001_04 |
| ORD ID | ord-05f846309ebb430c9ce70a7852c1dbbf |
| Quellennotiz | uspto-grants-2001_04 |