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- W2950997093 abstract "Abstract Nonpolar protic reaction media such as t -amyl alcohol allow the aliphatic, nucleophilic fluorination reaction of primary haloalkane systems to fluoroalkanes, using tetrabutylammonium fluoride (TBAF), to proceed chemo-selectively at a reasonable reaction rate under mild conditions to afford the fluoro-product in high yield. As an example, the nucleophilic fluorination of 2-(3-iodopropoxy)naphthalene ( 1a ) as the primary haloalkane model compound, with TBAF in acetonitrile as a polar aprotic solvent, CsF in t -amyl alcohol as a nonpolar protic solvent, and TBAF in t -amyl alcohol for 1 h provided 2-(3-fluoropropoxy)naphthalene ( 2a ) in 38, 5, and 76% yields, respectively." @default.
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- W2950997093 date "2010-04-13" @default.
- W2950997093 modified "2023-09-27" @default.
- W2950997093 title "ChemInform Abstract: Facile Nucleophilic Fluorination of Primary Alkyl Halides Using Tetrabutylammonium Fluoride in a tert-Alcohol Medium." @default.
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- W2950997093 doi "https://doi.org/10.1002/chin.201015090" @default.
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