Sources of common compounds: 4-Bromo-1-naphthonitrile

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 92616-49-4, name is 4-Bromo-1-naphthonitrile, A new synthetic method of this compound is introduced below., Formula: C11H6BrN

2-[(1H-Indol-2-yl)hydrazino]acetic acid methyl ester (2.2 g), 4-bromo-1-naphthalenecarbonitrile (2.3 g), CuI (1.0 g), Cs2CO3 (3.0 g),Dimethyl glycine (500 mg) was added to DMSO (50 mL) and replaced by argon gas. The reaction was stirred at 130 C for 12 h.After cooling to room temperature, ethyl acetate and saturated water were added to separate the layers. The ethyl acetate phase was washed twice with saturated brine, dried over anhydrous sodium sulfate and filtered.Concentration under reduced pressure and purification by column chromatography (eluent: dichloromethane:methanol = 10:1, v:v) gave 0.9 g of pure product in 24% yield.

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.