Formic Acid → Methyl 3-Formamidyl-2-methyl-4-methylsulfanylbenzoate
Reaktionsgleichung
[NH2:1][C:2]1[C:3]([CH3:14])=[C:4]([CH:9]=[CH:10][C:11]=1[S:12][CH3:13])[C:5]([O:7][CH3:8])=[O:6].[CH:15](O)=[O:16]>C(OC(=O)C)(=O)C>[CH:15]([NH:1][C:2]1[C:3]([CH3:14])=[C:4]([CH:9]=[CH:10][C:11]=1[S:12][CH3:13])[C:5]([O:7][CH3:8])=[O:6])=[O:16]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
At 40° C., 4.75 g of methyl 3-amino-2-methyl-4-methylsulfanylbenzoate (0.05 mol) were added a little at a time to a mixture of 30 ml of acetic anhydride and 2.2 g of formic acid (0.05 mol). After 5 h, the solution was allowed to cool and poured into ice-water, and the mixture was extracted exhaustively with methylene chloride. The organic phases were washed and dried, and the solvent was subsequently removed. Yield: 4.7 g (0.044 mol).
Aufarbeitung
- temperatureto cool
- extractionthe mixture was extracted exhaustively with methylene chloride
- washThe organic phases were washed
- customdried
- customthe solvent was subsequently removed
Quellen und Nachweise
- ORD-Eintrag
- ord-7c259bcd7d5f46efb7af8313d7eae164
- Quelldatensatz
- uspto-grants-2003_04
- Patentnummer
- US06541423B1
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