Phenylacetaldehyde → HCID 19016751, Verbindung
Reaktionsgleichung
[N+]([O-])(O)=O.[N+:5]([O-])(O)=O.[C:9]([OH:18])(=O)[CH:10]([CH:12]([C:14]([OH:16])=[O:15])O)O.[C:19]1([CH2:25][CH:26]=O)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.C(=O)=O.CC(C)=O.[OH-:35].[NH4+:36]>>[CH2:25]([C:26]1[NH:36][C:12]([C:14]([OH:16])=[O:15])=[C:10]([C:9]([OH:18])=[O:35])[N:5]=1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1Komponenten
5
Versuchsvorschrift
Tartaric acid dinitrate (0.67 mol) was neutralized to congo red test paper with concentrated ammonium hydroxide (500 mL). Additional concentrated ammonium hydroxide (50 mL) was added followed by a phenylacetaldehyde solution [previously prepared by the careful addition of phenylacetaldehyde (3.5 mol) to concentrated ammonium hydroxide (250 mL) with ice bath cooling]. The dry ice-acetone bath was replaced with ice-water and the reaction mixture was allowed to warm to room temperature over 16 hours. The precipitate was filtered, resuspended in water (400 mL) and stirred, filtered and the solid was washed with water (3×75 mL), methanol (2×40 mL) and ether (2×40 mL), then dried under vacuum to give 2-benzyl-4,5-imidazoledicarboxylic acid.