Angewandte
Chemie
DOI: 10.1002/anie.201500902
Ether Synthesis
Alkyl Aryl Ether Bond Formation with PhenoFluor**
Xiao Shen, Constanze N. Neumann, Claudia Kleinlein, Nathaniel W. Goldberg, and
Tobias Ritter*
Abstract: An alkyl aryl ether bond formation reaction between
phenols and primary and secondary alcohols with PhenoFluor
has been developed. The reaction features a broad substrate
scope and tolerates many functional groups, and substrates that
are challenging for more conventional ether bond forming
processes may be coupled. A preliminary mechanistic study
indicates reactivity distinct from conventional ether bond
formation.
E
thers are common,[1] yet their synthesis is often challenging.
Simple ethers are readily made through the Williamson ether
synthesis, which was developed more than 150 years ago,[2] but
even for moderately complex ethers, such as those derived
from secondary alcohols, the Williamson synthesis often fails
owing to low reactivity and undesired side reactions, such as
elimination.[2] Transition-metal-catalyzed or -mediated cross-
coupling reactions, exemplified by Ullmann,[3] Chan–Lam–
Evans,[4] and Buchwald–Hartwig couplings,[5] are powerful
methods for ether bond formation. Functionally complex
secondary alcohols, however, are challenging substrates for
these transition-metal-catalyzed reactions as well. The direct
coupling between phenols and alcohols for alkyl aryl ether
bond formation is appealing and orthogonal to other cross-
coupling approaches. The Mitsunobu reaction has been
developed for this purpose, and a large substrate scope has
been demonstrated.[6,7] However, several substrate classes,
such as salicylaldehydes, are not tolerated, and general
alcohol–alcohol cross-couplings are deemed challenging
owing to the high pKa values of typical alcohols.[8] Likewise,
the direct coupling of phenols and 2,2,2-trifluoroethanol in
a Mitsunobu reaction has not been reported. Herein, we
report a new approach to alkyl aryl ether formation through
the use of the reagent PhenoFluor (Scheme 1). The reaction
provides a conceptually different, promising reactivity profile,
possibly enabled by the tight ion pairing of key intermediates.
Our strategy distinguishes itself by operational simplicity—
phenols and alcohols can be used directly—and a large
substrate scope, which includes salicylaldehydes and 2,2,2-
trifluoroethanol. An example of selective glycosylation is also
Scheme 1. Fluorination and etherification reactions with PhenoFluor.
Boc=tert-butyloxycarbonyl, TMS=trimethylsilyl.
shown, further demonstrating the potential synthetic appli-
cations.
PhenoFluor is a commercially available deoxyfluorination
reagent for both alcohols and phenols, with a larger demon-
strated substrate scope than any other deoxyfluorination
reagent.[9] We speculated that instead of fluoride, phenolates
or alcoholates might act as nucleophiles to provide ethers if
the fluoride ions were effectively trapped by silanes.[10] The
reaction of an equimolar mixture of alcohol 2a and
4-fluorophenol with PhenoFluor and TMS-imidazole
(2 equiv) in dioxane at 608C for 21 hours afforded ether 3a
in 61% yield (Scheme 1; for reaction optimization, see the
Supporting Information). Without the addition of TMS-
imidazole, less than 1% of ether 3a was formed, and
deoxyfluorination of alcohol 2a was observed. The yield of
the ether bond formation could be increased by using the silyl
ethers of phenol 1a and alcohol 2a, but for operational
simplicity, we opted to develop the ether bond formation
directly from phenols and alcohols.
[*] Dr. X. Shen, C. N. Neumann, C. Kleinlein, N. W. Goldberg,
Prof. Dr. T. Ritter
Department of Chemistry and Chemical Biology
Harvard University
12 Oxford St., Cambridge, MA 02138 (USA)
E-mail: ritter@chemistry.harvard.edu
[**] We thank Teppei Fujimoto for the synthesis of PhenoFluor, Filippo
Sladojevich for helpful discussions, and the NIH (NIH-NIGMS
GM088237) for financial support.
Supporting information for this article is available on the WWW
Angew. Chem. Int. Ed. 2015, 54, 1 – 5
ꢀ 2015 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
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