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Author: Subject: Alternative Solvent for Allylbenzene and Allyltoluene synthesis
plutonium243
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[*] posted on 26-1-2023 at 17:31
Alternative Solvent for Allylbenzene and Allyltoluene synthesis


I'm looking for an alternative, and Ideally more common, high temperature solvent to use for the catalytic synthesis of allylaromatic hydrocarbons. In the paper I read (DOI: 10.1007/BF00845602), they added the hydrocarbon (say toluene or benzene) and catalyst of zinc chloride to a solution of allyl alcohol and either n-nonane or n-undecane, and then boiled until completion at ~108-120° C. Due to the high boiling point of toluene, they managed to run it solvent free, however all of their runs required undecane for the benzene version. I looked around, and it seems that undecane is somewhat rare and rather pricy. Can anyone think of a more common (and ideally less expensive) solvent that can be used. I was thinking using something like DMSO, as it seems to be miscible with benzene, dissolve both allyl alcohol and zinc chloride, and has a boiling point well above what is required. Does anyone know if there is any problems in using it? Alternatively, dodecane was more accessible, although still quite far from ideal. I would assume that there should be no problems with it instead, right?
Any suggestions would be much appreciated.
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[*] posted on 26-1-2023 at 17:48


If you use an alkyl halide instead of an alcohol, you can often get away with dichloromethane and FeCl3.



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plutonium243
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[*] posted on 27-1-2023 at 08:27


Wait, an alkyl halide and not an allyl halide? I would think that something like, say, propyl chloride would react to produce propyl or isopropyl benzene rather than allylbenzene. Also do the chlorides work well, since they seem more common than the bromides?
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[*] posted on 27-1-2023 at 09:33


I use t-butyl chloride/FeCl3 in dichloromethane. Allyl chloride would probably work just as well because allyl cations are resonance stabilized. A secondary or primary alkyl chloride would probably not work as well (but I haven't tried them).



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