2-Azidobenzoic acid → HCID 178423533, Verbindung

Reaktionsgleichung

[Na].[CH3:2][C:3]1[O:7][N:6]=[C:5]([CH2:8][C:9]#[N:10])[CH:4]=1.[N:11]([C:14]1[CH:22]=[CH:21][CH:20]=[CH:19][C:15]=1[C:16]([OH:18])=O)=[N+:12]=[N-:13]>CCO>[CH3:2][C:3]1[O:7][N:6]=[C:5]([C:8]2[N:13]=[N:12][N:11]3[C:14]4[C:15](=[CH:19][CH:20]=[CH:21][CH:22]=4)[C:16](=[O:18])[NH:10][C:9]=23)[CH:4]=1

Komponenten

Versuchsvorschrift

Sodium (0.2 g, 8.6 mmol) was dissolved in EtOH (9 mL) and (5-methylisoxazol-3-yl)acetonitrile (0.65 g, 5.3 mmol) was added. The solution was stirred for 15 min then a solution of 2-azidobenzoic acid (0.7 g, 4.3 mmol) in EtOH (7 mL) was added and the mixture stirred for 1 h. After this time the mixture was heated at reflux for 5 h. The suspension was then allowed to cool to room temperature and the solvent removed in vacuo. The residue was taken up in water and 1N citric acid was added to pH4. The resultant precipitate was collected by filtration, washed with water then dried in vacuo at 60° C. The title compound (0.92 g, 80%) was isolated as a colourless solid. 1HNMR (360 MHz, d6-DMSO) δ 2.51 (3H, s), 6.83 (1H, q, J=0.8 Hz), 7.72 (1H, d of t, J=8.1 and 1.0 Hz), 8.01 (1H, d of t, J=7.5 and 1.4 Hz), 8.24 (1H, dd, J=8.0 and 1.3 Hz), 8.36 (1H, d, J=8.0 Hz), 12.16 (1H, br s).