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Regarding the halogen substituents on benzene

2009-03-09View Original

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My goal is to replace the chlorine atom on the chloro-*** group, but in the end some of it gets replaced by a nitro group. What methods can be used to minimize this reaction as much as possible? Has anyone had a similar experience? Could you offer some advice? Thank you~ By the way, one more question: in the conditions for such reactions, does temperature have a greater impact or pressure? This post was last edited by zhangyong6404 on 2009-3-9 13:17.]
Reply #22009-03-09
The original poster didn’t specify enough, so I can’t give you any advice! ! !
Reply #32009-03-09
More specifically: Ammonia is used to react with chloro*** in order to replace the chlorine atoms, but ultimately some of those chlorine atoms are not replaced; instead, the nitro groups are replaced. I want to reduce this amount of reaction that occurs in such cases – are there any methods I can use for this?
Reply #42009-03-09
The first problem is easy to solve – one just needs to choose a good catalyst, one that reduces side reactions and increases the conversion rate. However, such catalysts are not easy to find. I won’t answer the second question either, because your description isn’t clear – what state is the reaction system in? Liquid? Gaseous? Is there a catalyst? How is the catalyst’s performance? How does activity change under the influence of temperature and pressure? I don’t know, so it’s hard to answer!
Reply #52009-03-09
For certain reasons that I can’t explain in detail, there are a few points that can be mentioned: there is no catalyst, the reaction takes place in a vapor-liquid mixture phase, and control is achieved only through adjustments to temperature and pressure. I’m unable to explain anything else; I’m sorry~:(
Reply #62009-03-09
To put it simply, I’d like to know some methods for controlling the substitution of halogens on the benzene ring, especially in amination reactions. I was wondering if any of you experienced professionals have any guidance on this topic :)
Reply #72009-03-09
For the reaction with chloro***, you can use NH3/CH3COONH4 at 170 degrees Celsius for 6 hours. The presence of NH4+ increases the concentration of NH3, which facilitates the progress of the reaction
Reply #82009-03-09
Other factors that also promote the reaction, aside from those already mentioned… The question is vague, so the answer can only be vague as well
Reply #92012-07-29
Industrially, ammonia water is reacted with perchloro*** under high temperature and pressure 222222
Reply #102012-08-23
Is the poster carrying out the amination reaction of chloro***? This process is quite mature, but there are still key control points; I have carried out such reactions before.

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