Hydrochloric Acid → HCID 86751213, Verbindung
Reaktionsgleichung
C([NH:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]([CH3:14])([CH3:13])[CH3:12])=[CH:7][C:6]=1[Br:15])(=O)C.[ClH:16]>C(O)C>[ClH:16].[Br:15][C:6]1[CH:7]=[C:8]([C:11]([CH3:14])([CH3:13])[CH3:12])[CH:9]=[CH:10][C:5]=1[NH2:4]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 24.33 g (90 mmol) of N-acetyl-2-bromo-4-tert-butyl aniline in 73.5 ml of 95% ethanol and 46 ml of concentrated hydrochloric acid is heated under reflux one hour. Then the mixture is cooled and the product is filtered, washed with cold 95% ethanol and dried. The yield of title compound is 21.75 g (91%).
Aufarbeitung
- temperatureunder reflux one hour
- temperatureThen the mixture is cooled
- filtrationthe product is filtered
- washwashed with cold 95% ethanol
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-5875059ff93643f683c83cfc2abc72d8
- Quelldatensatz
- uspto-grants-1997_09
- Patentnummer
- US05663448
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