Reaktionsgleichung
[C:1]([C:5]1[CH:16]=[CH:15][C:8]([CH2:9][NH:10]C(=O)C[Cl:13])=[C:7]([OH:17])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2]>CCO.Cl>[ClH:13].[NH2:10][CH2:9][C:8]1[CH:15]=[CH:16][C:5]([C:1]([CH3:3])([CH3:2])[CH3:4])=[CH:6][C:7]=1[OH:17]Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 85 °C
Versuchsvorschrift
N-(4-tert-Butyl-2-hydroxybenzyl)-2-chloroacetamide (270.0 mg, 1.06 mmol) was dissolved in a mixture of EtOH (4.0 ml) and conc. HCl (1.3 ml). The mixture was stirred at 85° C. for 3.0 h. The solvents were removed under vacuum to afford 225 mg (98%) of the title compound.
Aufarbeitung
- customThe solvents were removed under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-5cb7005112394fe3a53e0b87f0577507
- Quelldatensatz
- uspto-grants-2013_04
- Patentnummer
- US08415333B2
Verknüpfte Notizen
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