The important role of 4-Bromo-3,5-bis(trifluoromethyl)aniline

The synthetic route of 4-Bromo-3,5-bis(trifluoromethyl)aniline has been constantly updated, and we look forward to future research findings.

Reference of 268733-18-2, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 268733-18-2, name is 4-Bromo-3,5-bis(trifluoromethyl)aniline belongs to bromides-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below.

Disodium phosphate 18.2 g (123 mmol) and tetrabutylammonium hydrogen sulfate 2.1 g (6.20 mmol) were dissolved in a 500 mL solution of acetone and dichloromethane, followed by the addition of 4-bromo-3,5-bis-trifluoromethyl aniline 10.0 g (32.5 mmol) dropwise with a oxone and the reaction solution was stirred for 1 hour at 0 C. Potassium hydroxide was added to maintain the acidity of the reaction solution between 7.5 and 8.5. After completion of the reaction, the solution was diluted with dichloromethane and washed with distilled water several times to remove salts. Magnesium sulfate was then added to the dichloromethane solution and the solvent was filtered then evaporated and the resulting reactant was passed through a silica column pale to give a light yellow compound, 1-bromo-4-nitro-2,6-bis(trifluoromethyl)benzene (8.05 g, 23.8 mmol 73.3% yield). [0103] Melting point: 56-57 C. [0104] 1H NMR (CDCl3, 400 MHz, ppm): 8.71 (s, 2H). [0105] 13C NMR (DMSO-d6, 100 MHz, ppm): 146.62, 132.48 (q, J=31.9 Hz), 126.71 (q, J=5.7 Hz), 125.63, 121.68 (q, J=272.9 Hz).

The synthetic route of 4-Bromo-3,5-bis(trifluoromethyl)aniline has been constantly updated, and we look forward to future research findings.

Reference:
Patent; Kim, Sang Youl; Kim, Sun Dal; Chung, Im Sik; US2015/45481; (2015); A1;,
Bromide – Wikipedia,
bromide – Wiktionary