Adding a certain compound to certain chemical reactions, such as: 7417-18-7, 2-(2-Methoxyphenyl)ethanol, 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, Application In Synthesis of 2-(2-Methoxyphenyl)ethanol, blongs to alcohols-buliding-blocks compound. Application In Synthesis of 2-(2-Methoxyphenyl)ethanol
b) 4-Bromo-2-(2-hydroxyethyl)-anisole 35.72 g of tetrabutylammonium tribromide am added in portions to a solution of 10.7 g of 2-(2-hydroxyethyl)-anisole in 195 ml of dichloromethane and 130 ml of methanol. The reaction mixture is stirred for 150 minutes at room temperature and is then concentrated by evaporation in a rotary evaporator. The residue is partitioned between diethyl ether and water. The organic phases are combined, dried over magnesium sulfate and concentrated by evaporation, and the residue is purified by means of FC (dichloromethane), yielding the title compound: Rf (dichloromethane)=0.26; HPLC Rt =13.04 minutes.
At the same time, in my other blogs, there are other synthetic methods of this type of compound,7417-18-7, 2-(2-Methoxyphenyl)ethanol, and friends who are interested can also refer to it.
Reference:
Patent; Ciba-Geigy Corporation; US5559111; (1996); A;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts