five

Improved Synthesis of Larger Resorcinarenes

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https://figshare.com/articles/dataset/Improved_Synthesis_of_Larger_Resorcinarenes/3443360
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The synthesis of the larger resorcin­[5 and 6]­arene macrocycles [5]OMe and [6]OMe has been realized by a Lewis acid-catalyzed condensation of 1,3-dimethoxy-2-methylbenzene with paraformaldehyde in o-dichlorobenzene as the solvent. The methoxy-resorcin­[5 and 6]­arenes were quantitatively demethylated by treatment with BBr3 to obtain the corresponding macrocycles with free OH groups. X-ray studies showed that in the solid state both the conformation and the packing of [6]OMe and [5]OMe are driven by C–H···O, C–H···π, and π···π interactions.
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2016-06-27
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