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首页> 外文期刊>Organic & biomolecular chemistry >Alkoxycarbonylation of aryl iodides using gaseous carbon monoxide and pre-pressurized reaction vessels in conjunction with microwave heating
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Alkoxycarbonylation of aryl iodides using gaseous carbon monoxide and pre-pressurized reaction vessels in conjunction with microwave heating

机译:使用气态一氧化碳和预加压反应容器结合微波加热进行芳基碘化物的烷氧羰基化

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摘要

The microwave-promoted alkoxycarbonylation of aryl iodides using reaction vessels pre-pressurized with carbon monoxide is reported. Reactions are performed using 0.1 mol% palladium acetate as catalyst, DBU as base and are complete within 20-30 min. A range of aryl iodide substrates can be converted to the corresponding esters using this methodology. Primary and secondary alcohols work well whereas a tertiary alcohol substrate proves less reactive. The potential for scale-up of the reaction has also been explored.
机译:据报道,使用一氧化碳预加压的反应容器,微波促进了芳基碘化物的烷氧基羰基化反应。反应使用0.1 mol%乙酸钯作为催化剂,DBU作为碱进行,并在20-30分钟内完成。使用该方法可以将一定范围的芳基碘化物底物转化为相应的酯。伯醇和仲醇的效果很好,而叔醇底物的反应活性较低。还探索了扩大反应规模的潜力。

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