New downstream synthetic route of (2-Amino-3-bromophenyl)methanol

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 397323-70-5, (2-Amino-3-bromophenyl)methanol.

Related Products of 397323-70-5, The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 397323-70-5, name is (2-Amino-3-bromophenyl)methanol. This compound has unique chemical properties. The synthetic route is as follows.

To a solution of 139-2 (1.10 g, 5.44 mmol, 1 eq) in DCM (15 mL) was added Mn02 (4.73 g, 54.44 mmol, 10 eq). The mixture was stirred at 25 C for 1 hr. The reaction mixture was filtered and concentrated under reduced pressure to give 139-3 (1 g, crude) as a black oil.

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 397323-70-5, (2-Amino-3-bromophenyl)methanol.

Reference:
Patent; VIVACE THERAPEUTICS, INC.; KONRADI, Andrei W.; LIN, Tracy Tzu-Ling Tang; (472 pag.)WO2020/97389; (2020); A1;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Share a compound : 397323-70-5

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,397323-70-5, its application will become more common.

Adding a certain compound to certain chemical reactions, such as: 397323-70-5, (2-Amino-3-bromophenyl)methanol, 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, 397323-70-5, blongs to alcohols-buliding-blocks compound. Formula: C7H8BrNO

Step 2.; The benzylic alcohol (3.56g, 17.7 mmol) was taken up in DCM (80 mL) and treated with manganese dioxide (35g). The heterogeneous mixture was stirred at room temp for Ih, filtered and concentrated to provide the aldehyde (3.27g).

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,397323-70-5, its application will become more common.

Reference:
Patent; GILEAD SCIENCES, INC.; WO2007/11658; (2007); A1;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts