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Siddy
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This is a good find, the clean up seems a little complex due to the solubility of the di-phenol product.
If one were to be isolating the product to perform a methylenation reaction on the Catechol, could one not simply add hydroxide while the crude
product is still in the DCM/AlCl3 mix - or would the AlCl3 interfere?
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497
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Uhh you'd probably end up with a gelatinous mess of Al(OH)3...
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greenimp
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The hydroxy-vanillin is not soluble in the 5% aq. layer, nor the DCM layer (the vanillin is though)
Basically you get a solid, filter it out, and re-crystallize it. Not much easier than that.
The tetra-chloroehtane step boosts yields considerably.
green imp
Green Imp
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