Hydrochloric Acid → 1-(3'-Acetamino-phenyl)-2-amino-propane hydrochloride
Reaktionsgleichung
[NH2:1][C:2]1[CH:3]=[C:4]([CH2:8][CH:9]([NH2:11])[CH3:10])[CH:5]=[CH:6][CH:7]=1.[ClH:12].Cl.NC1C=C(CC(N)C)C=CC=1.[C:25](OC(=O)C)(=[O:27])[CH3:26]>C(O)(=O)C>[ClH:12].[NH:1]([C:2]1[CH:3]=[C:4]([CH2:8][CH:9]([NH2:11])[CH3:10])[CH:5]=[CH:6][CH:7]=1)[C:25]([CH3:26])=[O:27]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
15 gm of 1-(3'-amino-phenyl)-2-amino-propane were dissolved in glacial acetic acid, and ethereal hydrochloric acid was added to the solution. The resulting solution of 1-(3'-amino-phenyl)-2-amino-propane monohydrochloride was admixed with 15 ml of acetic acid anhydride, and the mixture was stirred for 10 minutes at room temperature. Thereafter, the reaction mixture was evaporated in a water aspirator vacuum, whereupon 1-(3'-acetamino-phenyl)-2-amino-propane hydrochloride crystallized out. Recrystallized from ethanol, the product had a melting point of 181°-183° C.
Aufarbeitung
- customThereafter, the reaction mixture was evaporated in a water
- customwhereupon 1-(3'-acetamino-phenyl)-2-amino-propane hydrochloride crystallized out
- customRecrystallized from ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-78fb070d71b24db581d9b9f315622885
- Quelldatensatz
- uspto-grants-1977_03
- Patentnummer
- US04015011
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