HRID54316
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
The title compound was prepared using an adaptation of the method of Cheeseman, G. W. H., J. Chem. Soc. 1171 (1962). A mixture of diethyl oxalate (1.15g, 7.91 mmol) and 1,2-diamino-3-bromo-5-trifluoromethylbenzene (200 mg, 0.95 mmol) was heated to reflux under N2 for 2 h. The reaction was allowed to cool to room temperature and the solid collected by vacuum filtration and rinsed with EtOH (15 mL). This white solid was dried in a drying pistol (0.05 torr, 78° C.) to yield 148.3 mg (60.7%). mp 301-304 (dec). 1H NMR (d6 -DMSO) δ7.28 (s, 1H, ArH), 7.56 (s, 1H, ArH), 11.7 (br s, 2H, NH). 19F NMR (C6F6 external standard, δ-162.9) δ-57.97 (s). EIHRMS calc. for C9H4BrF3N2O2 307.9408, found 307.9411.
WORKUP
后处理
- temperaturewas heated
- temperatureto reflux under N2 for 2 h
- filtrationthe solid collected by vacuum filtration
- washrinsed with EtOH (15 mL)
- customThis white solid was dried in a drying pistol (0.05 torr, 78° C.)
- customto yield 148.3 mg (60.7%)