Dimethylformamide → 6-Chloro-8-nitro-4H-benzo[1,4]oxazin-3-one

Reaktionsgleichung

[NH2:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([N+:9]([O-:11])=[O:10])[C:3]=1[OH:12].CN([CH:16]=[O:17])C.[C:18]([O-])([O-])=O.[K+].[K+]>>[Cl:8][C:6]1[CH:5]=[C:4]([N+:9]([O-:11])=[O:10])[C:3]2[O:12][CH2:18][C:16](=[O:17])[NH:1][C:2]=2[CH:7]=1

Komponenten

Edukt 3

HCID 6228Dimethylformamide

HCID 11430Potassium Carbonate

HCID 43482942-Amino-4-chloro-6-nitrophenol

Produkt 1

HCID 116515356-Chloro-8-nitro-4H-benzo[1,4]oxazin-3-oneAusbeute 19 %

Versuchsvorschrift

To a solution of 2-amino-4-chloro-6-nitrophenol (5 g, 26.5 mmol) in DMF (20 ml) ethylbromoacetate (3 ml, 26.5 mmol) and K2CO3 (4 g, 29.15 mmol) were added and the reaction was stirred at room temperature for 20 hours. The solvent was evaporated and the crude was dissolved in AcOEt (30 ml) and washed with NaOH 5%, water and brine. The organic phase was dried over sodium sulfate and concentrated under vacuum. The purification of the crude residue by crystallization from ether/AcOEt gave 1.13 g of a beige solid. Yield: 19%. 1HNMR (DMSO, 200 MHz) δ 4.79 (2H, s), 7.15 (1H, d, J=2.6 Hz), 7.66 (1H, d, J=2.8 Hz), 11.21 (1H, bs)