The important role of 14426-21-2

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it, 14426-21-2, Diethanolamine hydrochloride.

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps,and cheap raw materials. 14426-21-2, name is Diethanolamine hydrochloride. A new synthetic method of this compound is introduced below., SDS of cas: 14426-21-2

EXAMPLE 6 N,N-di-[2-(3,4,5-trimethoxybenzoyloxy)ethyl]taurine A mixture of 14 g of diethanolamine hydrochloride, 200 ml of dimethoxyethane and 47 g of 3,4,5-trimethoxybenzoyl chloride was left at ambient temperature for one night under agitation. The excess HCl was removed with a current of nitrogen, and the solution then evaporated under reduced pressure and taken up in 300 ml of anhydrous ethyl alcohol. 14 G of sodium ethoxide in 200 ml of absolute alcohol was added under cooling, then 21 g of sodium bromoethanesulphonate and 1.7 g of potassium iodide. After 120 hours at ambient temperature, the inorganic salts were filtered off and the solution concentrated under reduced pressure to a small volume. The mixture was then left to stand for one night, then filtered and crystallized from methanol. The product had a melting point of 179-182 C. and was identical to that obtained in Example 2.

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it, 14426-21-2, Diethanolamine hydrochloride.

Reference:
Patent; Laboratorio Chimico Farmaceutico CAUSYTH S.p.A.; US4259332; (1981); A;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts