Adding a certain compound to certain chemical reactions, such as: 79669-50-4, name is methyl 5-bromo-2-methyl-benzoate, belongs to esters-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 79669-50-4, Safety of methyl 5-bromo-2-methyl-benzoate
Step A Methyl 5-Bromo-alpha-(3-isopropylphenoxy)-o-toluate Treat a solution of 15 gm. (0.0655 mole) of methyl 5-bromo-o-toluate prepared according to Example 2 Step B in 75 ml. of carbon tetrachloride portionwise during 30 minutes with a mixture of 12.24 gm. (0.0688 mole) of N-bromosuccinimide and 130 mg. of benzoyl peroxide. Heat the resulting mixture at reflux for 3 hours. Cool to room temperature and separate the succinimide by filtration. Remove the solvent under vacuum to obtain methyl alpha,5-dibromo-o-toluate as a yellow residual oil.
At the same time, in my other blogs, there are other synthetic methods of this type of compound, methyl 5-bromo-2-methyl-benzoate, and friends who are interested can also refer to it.
Reference:
Patent; Merck & Co., Inc.; US4282365; (1981); A;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics