Is it possible to oxidize the alkyl substitutant with a dichromate ion to convert it into benzoic acid. I think I would add stoichiometric amounts of
potassium dichromate with toluene in excess and then reflux just like the permanganate method. Remove the layer with the potassium benzoate, and add
in some HCl to precipitate the Benzoic Acid. Then combine the benzoic acid with NaOH and distill the benzene.
Has anyone ever used potassium dichromate instead of permanganate?
Mirage |