Thionyl Chloride → (r)-Ethyl 3-amino-3-(3-nitrophenyl)propanoate hydrochloride salt
Reaktionsgleichung
Cl.[NH2:2][C@H:3]([C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([N+:16]([O-:18])=[O:17])[CH:11]=1)[CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6].N[C@H](C1C=CC=C([N+]([O-])=O)C=1)CC(O)=O.S(Cl)([Cl:36])=O>>[ClH:36].[NH2:2][C@@H:3]([C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([N+:16]([O-:18])=[O:17])[CH:11]=1)[CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6]Komponenten
4
Versuchsvorschrift
Using a procedure analogous to that used to prepare 34A, (S)-3-amino-3-(3-nitrophenyl)propanoic acid (2.1 g, 10 mmol) was reacted with thionyl chloride to 10 afford 39A (2.75 g, 99%) as a white solid. MS (ESI) m/z 239.08 (M+H)+.