Reductive alkylation of perfluorocarboxylic acid esters with CCl3F or CCl4 and synthesis of higher linear perfluoroketones

被引：7

作者：

Zeifman, YV ^{[1
]}

Postovoi, SA ^{[1
]}

机构：

[1] Russian Acad Sci, AN Nesmeyanov Organoelement Cpds Inst, Moscow 119991, Russia

来源：

JOURNAL OF FLUORINE CHEMISTRY | 2004年 / 125卷 / 12期

关键词：

perfluorocarboxylic acid esters; reductive alkylation; higher linear perfluoroketones; synthesis;

D O I：

10.1016/j.jfluchem.2003.11.008

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Barbier-type reductive alkylation of perfluorocarboxylic acid esters (I) with CFCl3 and activated Al was successfully performed to give alpha,alpha-dichloroperfluoroketones (U). A similar reaction of CF3COOEt with CCl4 and Al provided a convenient synthesis of CF3COCCl3. Ketones (II) were fluorinated further with SbF5 to form higher linear perfluoroketones (IX). An alternative approach to the synthesis of ketones (IX) was proposed by reductive perfluoroalkylation of esters (I) under the action of RFI and Al. (C) 2003 Elsevier B.V. All rights reserved.

引用

页码：1815 / 1819

页数：5

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