With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.1121-22-8,trans-Cyclohexane-1,2-diamine,as a common compound, the synthetic route is as follows.
General procedure: A solution of phenyl salicylate (2.13 g, 9.9 mmol) in 2-propanol (30 mL) was added to a 2-propanol solution (10 mL) containing 1,2-diamino-2-methylpropane (0.93 g, 10.6 mmol) dropwise with stirring. The mixture was stirred overnight at room temperature. The resulting white precipitate was collected by filtration, washed with 2-propanol and diethyl ether, and dried in vacuo., 1121-22-8
1121-22-8 trans-Cyclohexane-1,2-diamine 43806, achiral-catalyst compound, is more and more widely used in various fields.
Reference£º
Article; Mitsuhashi, Ryoji; Suzuki, Takayoshi; Sunatsuki, Yukinari; Kojima, Masaaki; Inorganica Chimica Acta; vol. 399; (2013); p. 131 – 137;,
Chiral Catalysts
Chiral catalysts – SlideShare