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A convenient and practical method for the selective preparation of deuterofluorocarbons

机译:一种方便实用的选择性制备氘代氟碳化合物的方法

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摘要

A detailed study of the development of efficient and practical conditions for the selective synthesis of 1-deuterononafluorobutane from 1-iodononafluorobutane is reported. The optimal conditions involve treatment of the iodo-precursor in D2O at similar to 170 degrees C in the presence of metallic zinc in a sealed Schlenk tube to give a 59% yield of 1-deutero-1,12,2,3,3,4,4,4-nonafluorobutane. The same method was applied successfully to two higher homologues to produce 1-deutero-1,1,2,2,3,3,4,4,5,5,5-undecafluoropentane and 1-deutero-1,1,2,2,32,4,4,5,5,6,6,6-tridecafluorohexane in yields of 64% and 56%, respectively. Surprisingly, even the non-perfluorinated product 6-deutero-1,1,1,2,2,3,3,4,4-nonafluorohexane could be synthesized in 69% yield with this method. (C) 2015 The Authors. Published by Elsevier B.V.
机译:报道了对从1-碘代氟代氟代烷选择性合成1-氘代氟代氟代烷的有效和实用条件发展的详细研究。最佳条件是在密封的Schlenk管中在金属锌存在下,在类似于170摄氏度的D2O中处理碘前体,以产生59%的1-氘1,1,2,2,3,3, 4,4,4-九氟丁烷。成功地将相同方法应用于两个较高的同系物,生成1-deutero-1,1,2,2,3,3,4,4,5,5,5,5-十一碳氟戊烷和1-deutero-1,1,2, 2,32,4,4,5,5,6,6,6,6-三氟硼己烷的产率分别为64%和56%。出乎意料的是,用这种方法甚至可以以69%的产率合成6-全氟代的1,1,2,2,3,3,4,4-九氟己烷。 (C)2015作者。由Elsevier B.V.发布

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