2-Amino-5-chlorobenzophenone

Application
A metabolite of Diazepam; it had a much weaker anticonvulsant effect.

Pharmaceutical intermediates. Manufacture of drugs such as Librium and Valium.
Environmental impact
Slightly hazardous to water, do not allow undiluted or large quantities to come into contact with groundwater, waterways or sewage systems, and do not discharge materials into the surrounding environment without government permission

Properties and Stability
Stable at ambient temperature and pressure, avoid contact with oxides

Storage methods
Keep container tightly closed and store in a cool, dry place in a tightly packed container.

Synthesis method
(1) Produced by the reaction of p-chloroaniline with benzoyl chloride. Add p-chlorobenzene to the glass-lined reaction pot at 70°C or below, put in anhydrous zinc chloride, add benzoyl chloride dropwise with stirring, then raise the temperature, hold at 195-205°C for 2h, wash five times with hot water at 90-95°C (the water layer and the washing solution recover benzoic acid and zinc chloride) at about 100°C, add sulfuric acid slowly, hold at 142°C for 40min. The solids are precipitated in water. Under stirring, the pH is adjusted with liquid alkali to no higher than 1 and filtered at 20-25 °C. The filtrate is recovered as p-chloroaniline. The filter cake is mixed and suspended in water, neutralised to pH=6, filtered dry, washed with water to neutral and dried to obtain the crude product. Then add 6-7 times ethanol, 6% activated carbon, reflux for 30min, filter and crystallize, dry to obtain the fine product. (2) p-Nitrochlorobenzene and cyanobenzyl ring combination to obtain isoxazole, then open the ring, the reduction to obtain.