Tetrahydrofuran → Ethyl (2-methoxy-6-nitrophenyl)carbamate
Reaktionsgleichung
Cl[C:2]([O:5][C:6](Cl)=[O:7])(Cl)Cl.[CH3:9][O:10][C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([N+:17]([O-:19])=[O:18])[C:12]=1[NH2:20].[CH2:21]1COCC1>>[CH3:9][O:10][C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([N+:17]([O-:19])=[O:18])[C:12]=1[NH:20][C:6](=[O:7])[O:5][CH2:2][CH3:21]Komponenten
4
Versuchsvorschrift
17.1 mL (0.141 mol) trichloromethylchloroformate are added dropwise at reflux temperature to a solution of 23.8 g (0.142 mol) 2-methoxy-6-nitro-phenylamine in 300 mL THF and then the mixture is stirred for 4 hours at this temperature. The solvent is distilled off and the residue is stirred with isopropanol, during which time a yellow solid is precipitated. Yield: 25.0 g (73%); mass spectroscopy: [M+H]+=241.
Aufarbeitung
- distillationThe solvent is distilled off