Reaktionsgleichung
[CH3:1][N:2]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[CH2:3][C:4]([OH:6])=[O:5].[C:13]([Cl:16])(=O)C>CO>[ClH:16].[CH3:13][O:5][C:4](=[O:6])[CH2:3][N:2]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[CH3:1]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Prepared by Method A of Example 19 but using N-methyl-phenylglycine (prepared in turn from 2-chlorophenylacetic acid and methylamine) (3.5 g) methanol (20 ml) and acetyl chloride (40 ml) over 48 hours. The title compound was obtained in 94% yield, after trituration with methanol, as a white solid.
Aufarbeitung
- customPrepared by Method A of Example 19
- customover 48 hours
Quellen und Nachweise
- ORD-Eintrag
- ord-3f0ae84401de4753b2d31985f3ef5bd9
- Quelldatensatz
- uspto-grants-2000_04
- Patentnummer
- US06048852
Verknüpfte Notizen
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