HRID1369345
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
The procedure of Example 1 is repeated using 3.9 g (25 mmol) of 1-oxyl-2,2,6,6-tetramethylpiperidine, and 7.84 g (76 mmol) of tert-butyl nitrite, 24 mg (0.25 mmol) of copper(II) chloride, 120 mL of acetonitrile and 4.65 g (50 mmol) of aniline at 65° C. The crude product is purified by vacuum flash chromatography (heptane) to give 4.2 g of the title compound as a colorless oil in a 72.4% yield.
WORKUP
后处理
- customat 65° C
- customThe crude product is purified by vacuum flash chromatography (heptane)