Sources of common compounds: 2,5-Dibromo-1-chloro-3-fluorobenzene

At the same time, in my other blogs, there are other synthetic methods of this type of compound, 2,5-Dibromo-1-chloro-3-fluorobenzene, and friends who are interested can also refer to it.

Synthetic Route of 1000572-88-2, As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 1000572-88-2 name is 2,5-Dibromo-1-chloro-3-fluorobenzene, This compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below.

An autoclave equipped with a stir bar was charged with 2,5-dibromo- l-chloro-3-fluorobenzene (5.0 g, 17.3 mmol), triethylamine (12.1 mL, 86.7 mmol), bis(diphenylphosphino)ferrocene)palladium(II) Chloride (0.86 mmol, 708 mg) and methanol (100 mL) was degassed with nitrogen for 10 min. Then the container was sealed and filled with CO to 400 psi. The reaction mixture was heated at 100 C with stirring for 12 hours. The reaction mixture was filtered through Celite, washed with MeOH, and the filtrate was concentrated. The crude product was purified by silica gel chromatography (0-10% EtOAc/hexane) to afford the title compound as a colorless oil which solidified in high vacuum (3.06 g, 71% yield). ¾ NMR (400 MHz, CDC13) delta 7.90 (s, 1H), 7.69 (dd, J = 9.0, 1.2 Hz, 1H), 3.99 (s, 3H), 3.95 (s, 3H). LCMS (APCI+) 247.0[M+H]+

At the same time, in my other blogs, there are other synthetic methods of this type of compound, 2,5-Dibromo-1-chloro-3-fluorobenzene, and friends who are interested can also refer to it.

Reference:
Patent; F. HOFFMANN-LA ROCHE AG; BLENCH, Toby; ELLWOOD, Charles; GOODACRE, Simon; LAI, Yingjie; LIANG, Jun; MACLEOD, Calum; MAGNUSON, Steven; TSUI, Vickie; WILLIAMS, Karen; ZHANG, Birong; WO2012/35039; (2012); A1;,
Chloride – Wikipedia,
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