首页> 外文期刊>Tetrahedron >Zeolite-catalyzed acylation of heterocyclic compounds - VI. One-step synthesis of 3(benzofuran-2-carbonyl)pentane-2,4-dione from 2-acetylbenzofuran over HY-zeolite.
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Zeolite-catalyzed acylation of heterocyclic compounds - VI. One-step synthesis of 3(benzofuran-2-carbonyl)pentane-2,4-dione from 2-acetylbenzofuran over HY-zeolite.

机译:沸石催化的杂环化合物的酰化反应-VI。在HY沸石上由2-乙酰基苯并呋喃一步合成3(苯并呋喃-2-羰基)戊烷-2,4-二酮。

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摘要

The reaction between 2-acetylbenzofuran and acetic anhydride at 60 degrees C in the presence of HY-zeolite (Si/Al = 16) led to a single final product:3-(benzofuran-2-carbonyl)pentane-2,4-dione resulting from two consecutive acylation steps on the side chain. It was obtained in a 90% purity at around 50% conversion of 2-acetylbenzofuran. Other minor products and intermediates were also identified. A mechanism is proposed to account for the formation of the various products. (C) 1998 Elsevier Science Ltd. All rights reserved. [References: 21]
机译:2-乙酰基苯并呋喃与乙酸酐在60°C下在HY沸石(Si / Al = 16)存在下反应生成单个最终产物:3-(苯并呋喃-2-羰基)戊烷-2,4-二酮由侧链上两个连续的酰化步骤产生。以2-乙酰基苯并呋喃的约50%的转化率以90%的纯度获得了它。还确定了其他次要产品和中间体。提出了一种机制来解释各种产品的形成。 (C)1998 Elsevier ScienceLtd。保留所有权利。 [参考:21]

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