Tert-Butylamine → HCID 13748402, Verbindung
Reaktionsgleichung
[O:1]1[CH2:3][CH:2]1[C:4]1[N+:9]([O-:10])=[C:8]2[CH2:11][O:12][CH:13]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[O:14][C:7]2=[CH:6][CH:5]=1.[C:21]([NH2:25])([CH3:24])([CH3:23])[CH3:22]>CO>[OH:1][CH:2]([C:4]1[N+:9]([O-:10])=[C:8]2[CH2:11][O:12][CH:13]([C:15]3[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=3)[O:14][C:7]2=[CH:6][CH:5]=1)[CH2:3][NH:25][C:21]([CH3:24])([CH3:23])[CH3:22]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To 15.0 g. (0.055 mole) of 6-(1,2-epoxyethyl)-2-phenyl-4H-1,3-dioxino[5,4-b]pyridine N-oxide in 200 ml. of methanol was added 30 ml. tert-butylamine and the resulting reaction mixture was heated to the reflux temperature for 3 hours. Solvent and excess tert-butylamine were removed in vacuo to give 13.4 g. (73.6%) of 6-(1-hydroxy-2-tert-butylaminoethyl)-2-phenyl-4H-1,3-dioxino[5,4-b]pyridine N-oxide after recrystallization from ethyl acetate: m.p. 165°-168° C.