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chlorination of phenylpropenes


aminationman

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would a PTC be absolutely necessary for a beta-chlorination of the propenyl benzenes working with 37% hcl? also would an aprotic non polar solvent be required to eliminate polymerization of the phenylpropene? would gaseous hcl bubbled through the phenylpropene be a better way to go than two phase and PTC?

how would this compound then fair under a 10x molar excess of NH3 in MEOH stored at room temp for a week or so? primary amine? expected yeilds?

 

any advice would be much appreciated

 

thanks aminationman

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I agree with the other two, this is a very suspicious synthesis. If you can show that this isn't a means to produce illicit substances, we'd be happy to help. If not, I have to ask how on earth you thought pulling the proverbial wool over the eyes of the professional chemists who use this site would actually work?

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