Ammonia → HCID 19774727、化合物
反応式
CO[C:3]1[C:4]([N+:34]([O-:36])=[O:35])=[C:5]([C:15]2[C:20]([N+:21]([O-:23])=[O:22])=[CH:19][C:18]([N+:24]([O-:26])=[O:25])=[C:17]([NH:27][CH2:28][CH2:29][OH:30])[C:16]=2[N+:31]([O-:33])=[O:32])[C:6]([N+:12]([O-:14])=[O:13])=[CH:7][C:8]=1[N+:9]([O-:11])=[O:10].[NH3:37]>CO>[NH2:37][C:7]1[C:6]([N+:12]([O-:14])=[O:13])=[C:5]([C:15]2[C:20]([N+:21]([O-:23])=[O:22])=[CH:19][C:18]([N+:24]([O-:26])=[O:25])=[C:17]([NH:27][CH2:28][CH2:29][OH:30])[C:16]=2[N+:31]([O-:33])=[O:32])[C:4]([N+:34]([O-:36])=[O:35])=[CH:3][C:8]=1[N+:9]([O-:11])=[O:10]参加物
4
実験手順
A mixture of 0.55 g (0.0011 mole) of 3-methoxy-3'-(2-hydroxyethylamino)-2,2',4,4',6,6'-hexanitrobiphenyl and 10 ml of methanol was stirred in an ice bath while a solution of gaseous ammonia in methanol was added until the mixture remained basic to damp pH paper. The mixture was then kept basic with ammonia as it was stirred at room temperature for 3 hours. After standing overnight, the insoluble yellow solid product 3-amino-3'-(2-hydroxyethylamino)-2,2',4,4',6,6'-hexanitrobiphenyl was removed to give 0.45 g (85%), mp 246° C. dec; 1H NMR (acetone-d6 +D2O): 3.28 (t, 2H), 3.90 (t, 2H), 9.50 (overlapping s, 2H).