Adding a certain compound to certain chemical reactions, such as: 143-24-8, name is 2,5,8,11,14-Pentaoxapentadecane, belongs to ethers-buliding-blocks compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 143-24-8, Recommanded Product: 143-24-8
(a) 7-Benzyl-6,7,8,9-tetrahydro-5H-pyrazino[2,3-d]-azepine hydrochloride 10.9 gm (30 mmols) of 1-benzyl-2,3,6,7-tetrahydro-4,5-bis(trimethylsilyloxy)-azepine were dissolved in a mixture of 20 ml ethylenediamine and 30 ml tetraethyleneglycol dimethyl ether, and air was passed through the solution at 120 C. for eight hours. Thereafter, the reaction mixture was poured into water, and the aqueous composition was extracted with chloroform. The chloroform extract solution was dried and evaporated, and the residue was chromatographically purified on silicagel with methanol as the mobile phase. Subsequently, the hydrochloride was precipitated from ethanol with ethanolic hydrochloric acid. Yield: 2.4 gm (29% of theory) Melting point: 244-247 C. Calculated: C: 65.33%; H: 6.58%; N: 15.24%; Cl: 12.85% Found: C: 65.01%; H: 6.42%; N: 14.89%; Cl: 12.31%.
In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 2,5,8,11,14-Pentaoxapentadecane, other downstream synthetic routes, hurry up and to see.
Reference:
Patent; Dr. Karl Thomae Gesellschaft mit beschrankter Haftung; US4409220; (1983); A;,
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem