Analyzing the synthesis route of 1662-01-7

The synthetic route of 1662-01-7 has been constantly updated, and we look forward to future research findings.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.1662-01-7,4,7-Diphenyl-1,10-phenanthroline,as a common compound, the synthetic route is as follows.

A solution of (No.5-Ind) Mo (CO) 2 (3-C3H5) (0.20g, 0.65 mmol) in CH2C12 was treated with HBF4. Et2O (1 eq. ). After 10 minutes dme was added in excess and the reaction was left for 15 minutes. 0.27 g (0.8 mmol) of 4, 7-diphenil-1, 10-phenantroline were added and the reaction was left for 2 hours at room temperature. After concentration to about 5 ml and addition of Et20, a ruby complex precipitated. The mixture was filtered and the residue recrystallized from CH2CI2/Et2O (razz 90%). A drawing of the structure and physical data are given in Table 1., 1662-01-7

The synthetic route of 1662-01-7 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; IBET-INSTITUTO DE BIOLOGIA EXPERIMENTAL E TECNOLOGICA; WO2005/87783; (2005); A1;,
Metal catalyst and ligand design
Ligand Template Strategies for Catalyst Encapsulation – NCBI