YAKUGAKU ZASSHI
Online ISSN : 1347-5231
Print ISSN : 0031-6903
ISSN-L : 0031-6903
縮合剤としてのポリ燐酸の応用に関する研究 (第4報)
カテコール, レゾルシン, レズアシロフエノン及びそれらのメチルエーテル類の核アシル化反応
中澤 浩一
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ジャーナル フリー

1954 年 74 巻 8 号 p. 836-839

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Nuclear acylated compounds were prepared by heating catechol, resorcinol, resacylophenones, and their methyl ethers with acetic or propionic acid, in the presence of polyphosphoric acid, for 10-20 minutes in a boiling water bath. Catechol, guaiacol, and veratrole yielded acylocatechols, acylovanillones, and acyloveratrones, while resorcinol and its mono- and dimethyl ethers easily gave resacylophenones, their 4- and 2-methyl ethers, and dimethyl ethers in a good yield. Resacylophenones gave 4, 6-diacylresorcinols and resacylophenone 4-methyl ethers gave 4, 6-diacylresorcinol monomethyl ethers. However, nuclear acylation of resacylophenone 2-methyl ethers was difficult and resacylophenone dimethyl ethers failed to undergo nuclear acylation.
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© by the PHARMACEUTICAL SOCIETY OF JAPAN
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