Scientific Study & Research: Chemistry & Chemical Engineering, Biotechnology, Food Industry (Dec 2011)

SYNTHESIS OF ALLYL PHENYL ETHER AND CLAISEN REARRANGEMENT

  • Gagik Torosyan,
  • Dezy Hovhannisyan

Journal volume & issue
Vol. 12, no. 4
pp. 425 – 428

Abstract

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It has been established the possibility for phenol allylation on natural zeolites and them analogs. Here is demonstrated the synthesis of allyl phenol, which has wide industrial applications. The offered method in comparison with the traditional methods has more advantages – higher selectivity, smaller material and power resources consumption. It has been obtained the mixture of allylating phenols (30%) in general with allyl phenyl ether (1) with 80% yields. At 600 K is obtained allylphenyl ether, at 700 K beginning the formation of allyl phenols, which is the result of direct C-allylation of the aromatic ring. It has been investigated the possibility of Claisen rearrangement in the same conditions. All of that are established by gas-liquid chromatography and liquid chromatography data.

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