Hydrochloric Acid → 5-Phenylsulphonamido-1,2,3,4-tetrahydroisoquinoline hydrochloride
Reaktionsgleichung
C([N:4]1[CH2:13][CH2:12][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][C:10]=2[NH:14][S:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)(=[O:17])=[O:16])[CH2:5]1)(=O)C.[ClH:24]>C(O)CCC>[ClH:24].[C:18]1([S:15]([NH:14][C:10]2[CH:9]=[CH:8][CH:7]=[C:6]3[C:11]=2[CH2:12][CH2:13][NH:4][CH2:5]3)(=[O:17])=[O:16])[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A stirred mixture of 2-acetyl-5-phenylsulphonamido-1,2,3,4-tetrahydroisoquinoline (9.4 g), hydrochloric acid (140 ml, 3.0M) and n-butanol (14 ml) was heated under reflux for 6 hours. The solvents were evaporated under reduced pressure and the residue was recrystallised from ethanol to give 5-phenylsulphonamido-1,2,3,4-tetrahydroisoquinoline hydrochloride as a white solid (7.8 g) m.p. 209°-21° C.