Adding a certain compound to certain chemical reactions, such as: 61367-62-2, 4-Bromo-3,5-dimethoxybenzyl alcohol, 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, Safety of 4-Bromo-3,5-dimethoxybenzyl alcohol, blongs to alcohols-buliding-blocks compound. Safety of 4-Bromo-3,5-dimethoxybenzyl alcohol
To a mixture of 4-bromo-3,5-dimethoxybenzylalcohol (44.5 g), triethylammonium benzyl chloride (2.05 g) and 20percent aqueous sodium hydroxide solution (288 g) was added diethyl sulfate (41.7 g) under ice-cooling, and the mixture was stirred overnight at 25-30°C. After stirring for 1 hour at 70°C, the mixture was cooled and extracted with toluene. The toluene layer was washed with water and saturated aqueous NaCl solution and dried over magnesium sulfate. The solvent was removed in vacuo to yield 4-bromo-3,5-dimethoxybenzyl ethyl ether (49.5 g) as colorless oil. MS (m/z): 276 (M++2), 274 (M+)
At the same time, in my other blogs, there are other synthetic methods of this type of compound,61367-62-2, 4-Bromo-3,5-dimethoxybenzyl alcohol, and friends who are interested can also refer to it.
Reference:
Patent; TANABE SEIYAKU CO., LTD.; WO2003/72536; (2003); A1;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts