首页> 外文期刊>The Journal of Organic Chemistry >Synthesis of α-halo-α,α-difluoromethyl ketones by a trifluoroacetate release/halogenation protocol
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Synthesis of α-halo-α,α-difluoromethyl ketones by a trifluoroacetate release/halogenation protocol

机译:三氟乙酸盐释放/卤化方案合成α-卤代-α,α-二氟甲基酮

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摘要

Three series of α-halo-α,α-difluoromethyl ketones are prepared from highly α-fluorinated gem-diols by exploiting the facile release of trifluoroacetate, followed by immediate trapping of the liberated α,α-difluoroenolate with an electrophilic chlorine, bromine, or iodine source. The products are typically isolated in good yields, even in the case of sensitive, α-iodo-α,α-difluoromethyl ketones. Also, we demonstrate that an α-iodo-α,α-difluoromethyl ketone will participate in a copper-promoted reaction to forge a new carbon-carbon bond.
机译:通过利用三氟乙酸的轻松释放,然后用亲电子氯,溴立即捕获释放的α,α-二氟烯酸酯,由高度α-氟化的宝石二醇制备三系列的α-卤代-α,α-二氟甲基酮。或碘源。即使在敏感的α-碘-α,α-二氟甲基酮的情况下,通常也以高收率分离出产物。另外,我们证明了α-碘-α,α-二氟甲基酮将参与铜促进的反应以形成新的碳-碳键。

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