Abstract
AbstractA one‐step synthesis of cryptand [2.2.2] containing three methylenyl substituents in a 25% yield from the reaction of triethanolamine and 3‐chloro‐2‐chloromethyl‐1‐propene is described. A similar cryptand was prepared in 56% yield by a two‐step process. One‐step syntheses of N,N‐hydroxyethyl‐diaza‐18‐crown‐6 and crown‐6 compounds containing two alkene functional groups are also described.
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