HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
m-Chloroperbenzoic acid → 2-(4-methylphenyl)-6-methylpyridine-N-oxide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | m-Chloroperbenzoic acid | HCID 70297 | — |
| Edukt | 2-Methyl-6-(4-methylphenyl)pyridine | HCID 603081 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 2-(4-methylphenyl)-6-methylpyridine-N-oxide | HCID 19430330 | 57,2% |
Reaktionsschritte
A solution of 2-(4-methylphenyl)-6-methylpyridine (4.5 g) in 100 ml of chloroform was cooled to 0° C., and m-chloroperbenzoic acid (7.7 g) in 50 ml of chloroform was added over a period of 15 minutes. The mixture was stirred at room temperature for 3 hours, then at 50° C. for 2 hours, followed by stirring overnight at room temperature. Solvent was evaporated to a small volume under reduced pressure, and the residue passed through an alumina column, eluting with 2% methanol in methylene chloride to remove benzoic acid. The eluate was flash-Chromatographed on silica gel, eluting with 5% methanol in methylene chloride, to yield 2.8 g of 2-(4-methylphenyl)-6-methylpyridine-N-oxide, m.p. 95° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05428037 |
| Quelldatensatz | uspto-grants-1995_06 |
| ORD ID | ord-c5f37f607fa446e491d9d67022356215 |
| Quellennotiz | uspto-grants-1995_06 |