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Author: Subject: Acquire trimesic acid.
goose
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[*] posted on 22-3-2022 at 09:49
Acquire trimesic acid.

All of the online sources of trimesic acid I can find are prohibitively expensive. Would a synthesis from toluene be the best option (The only problem with that is that I cannot get aluminum trichloride)?
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Tsjerk
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[*] posted on 22-3-2022 at 10:54


I had to Google that one, but how much do you need? And do you have a reference to the synth from toluene? If all you need is a little maybe you can work out something with in situ generated AlCl3?
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[*] posted on 22-3-2022 at 11:04


There’s some discussion in the benzene sticky thread about disproportionation of toluene to benzene and mesitylene using catalytic AlCl3, and some speculation about generating it in situ, but I don’t know if anyone ever got around to trying it, because I haven’t read all 14 pages of that thread.



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mackolol
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[*] posted on 22-3-2022 at 13:28


http://www.orgsyn.org/demo.aspx?prep=CV1P0341
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goose
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[*] posted on 23-3-2022 at 09:11


Quote: Originally posted by Tsjerk  
I had to Google that one, but how much do you need?

Not much, only 10-20ml.
Thanks Mackolol that route looks better than using methyl halides. Mesitylene to trimesic shouldn't be to bad, I plan on following a procedure for tolulene oxidation, except increasing the amount of KMnO4. That seems like the best option.
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Organikum
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[*] posted on 26-7-2022 at 11:47


Toluene (dry) + Aluminium (even fol works) + iodine. Boil boil boil and then boil it a little bit longer.

In situ formed AlI3 works even better then AlCl3, workup is by simple fractional distillation.


courtesy of Osmium at the HIVE

/ORG



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clearly_not_atara
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[*] posted on 27-7-2022 at 02:52


I have my doubts about Osmium but I think the chemistry there makes sense.



[Edited on 04-20-1969 by clearly_not_atara]
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