Artigo Revisado por pares

Direct and Convenient Conversion of Alcohols to Fluorides

2004; American Chemical Society; Volume: 6; Issue: 9 Linguagem: Inglês

10.1021/ol049672a

ISSN

1523-7060

Autores

Jingjun Yin, Devin S. Zarkowsky, David W. Thomas, Matthew M. Zhao, Mark A. Huffman,

Tópico(s)

Oxidative Organic Chemistry Reactions

Resumo

[reaction: see text] Directly mixing primary, secondary, and tertiary alcohols with nC(4)F(9)SO(2)F-NR(3)(HF)(3)-NR(3) in THF or MeCN results in convenient conversion to the corresponding fluorides in high yields. The readily available reagents are easy to handle, and the mild, almost neutral reaction conditions allow for excellent functional group compatibility. A NR(3)(HF)(3)/NR(3) ratio of </=1:2 gives the highest reactivity.

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