An alternative method for generating arynes from ortho-silylaryl triflates: Activation by cesium carbonate in the presence of a crown ether

Article abstract of DOI:10.3390/molecules200610131

An alternative method for generating arynes from ortho-silylaryl triflates using cesium carbonate and 18-crown-6 is reported. The method was efficiently applied to a variety of reactions between several arynes and arynophiles. We also demonstrated that the efficiency of aryne generation is significantly affected by the alkali metal countercation of the carbonate.

Full text of DOI:10.3390/molecules200610131

Molecules 2015, 20, 10131-10140; doi:10.3390/molecules200610131
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molecules
ISSN 1420-3049
www.mdpi.com/journal/molecules
Communication
An Alternative Method for Generating Arynes from
ortho-Silylaryl Triflates: Activation by Cesium Carbonate in the
Presence of a Crown Ether
Suguru Yoshida, Yuki Hazama, Yuto Sumida, Takahisa Yano and Takamitsu Hosoya *
Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering,
Tokyo Medical and Dental University, 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan;
E-Mails: s-yoshida.cb@tmd.ac.jp (S.Y.); yuki.h.05261986@gmail.com (Y.H.);
yuto.sumida@riken.jp (Y.S.); yano@acls.titech.ac.jp (T.Y.)
* Author to whom correspondence should be addressed; E-Mail: thosoya.cb@tmd.ac.jp;
Tel.: +81-3-5280-8000; Fax: +81-3-5280-8001.
Academic Editors: Daesung Lee and Hiroto Yoshida
Received: 1 May 2015 / Accepted: 28 May 2015 / Published: 1 June 2015
Abstract: An alternative method for generating arynes from ortho-silylaryl triflates using
cesium carbonate and 18-crown-6 is reported. The method was efficiently applied to
a variety of reactions between several arynes and arynophiles. We also demonstrated that the
efficiency of aryne generation is significantly affected by the alkali metal countercation of
the carbonate.
Keywords: aryne; ortho-silylaryl triflate; cesium carbonate; crown ether
1. Introduction
Arynes are highly reactive intermediates useful for preparing diverse aromatic compounds [1–8].
Novel transformations of arynes have been achieved and applied to the synthesis of a wide range of
complex aromatic compounds. In line with the growing importance of aryne chemistry, a variety of
methods and precursors to generate arynes have been developed. In particular, activation of ortho-silylaryl
triflates with a fluoride ion is one of the most widely-used methods for generating arynes [9]. Due to the
increased availability of ortho-silylaryl triflates [10,11], numerous transformations via arynes have been
developed based on this method [12–24].

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As a part of our studies focusing on highly strained alkynes, including arynes [24–34], we have been
working on a project to develop new aryne generation methods. For example, we have recently
succeeded in efficiently generating arynes from ortho-iodoaryl triflates bearing sensitive functional
groups using a trimethylsilylmethyl Grignard reagent as an activator [30,31,33] instead of conventional
activators such as n-butyllithium [35] or a turbo-Grignard reagent [36]. Herein, we report that cesium
carbonate, in the presence of a crown ether, serves in place of a fluoride ion as an efficient activator for
generating arynes from ortho-silylaryl triflates.
2. Results and Discussion
We first screened efficient conditions for generating benzyne from 2-(trimethylsilyl)phenyl triflate
(1a) without the use of a fluoride ion and in the presence of benzyl azide (2), which was employed as an
arynophile. Consequently, we found that cesium carbonate slowly triggers the generation of benzyne from
1a to afford benzotriazole 3 (Table 1, entries 1–4). While the reaction in tetrahydrofuran at 25 °C for 24 h
resulted in the generation of a trace amount of benzyne with the recovery of a significant amount of 1a
(entry 1), performing the reaction with heating at 60 °C improved the efficiency (entry 2). Further
improvement was observed by switching solvent from tetrahydrofuran to acetonitrile (entries 3 and 4).
After extensive screening of the conditions to further enhance the efficiency of benzyne generation from
1a using cesium carbonate, we found that addition of 18-crown-6-ether dramatically accelerates benzyne
generation, affording the product 3 in high yield, even when the reaction is performed at 25 °C (entry 5) [37].
Among the various solvents examined, tetrahydrofuran and 1,2-dimethoxyethane gave the best results
(entries 5–9). Conversely, generation of benzyne was not observed when cesium carbonate was replaced
by cesium bicarbonate (entry 10), which was previously used concomitantly with cesium carbonate and
18-crown-6 to generate benzyne from 2-(trimethylsilyl)phenyl nonaflate with moderate efficiency [38].
Moreover, the efficiency of the reaction was reduced when potassium carbonate and 18-crown-6, which
can retain a potassium cation inside the molecule, were used (entry 11). In this case, the yield of 3 was
improved by using an increased amount of 18-crown-6 (entry 12). Treatment of 1a with tripotassium
phosphate in the presence of 18-crown-6 also triggered benzyne generation, albeit slowly (entry 13).
Although the efficiency of benzyne generation from 1a mediated by cesium carbonate and 18-crown-6
was slightly inferior to the conventional methods using potassium fluoride and 18-crown-6 (entry 14) or
cesium fluoride alone (entry 15), the newly established conditions are worth exploring for optimization
of the reactions that use arynes generated from ortho-silylaryl triflates.
The optimized reaction conditions were applicable to the reactions between benzyne and
various arynophiles (Table 2). Diels–Alder reaction of benzyne generated from 1a with furan (4),
2,5-dimethylfuran (6), or N-phenylpyrrole (8) provided the corresponding cycloadducts 5a, 7, and 9,
respectively, in good yields (entries 1–3). Nitrone 10 also reacted with benzyne to afford cycloadduct 11
efficiently (entry 4). Amination of benzyne with morpholine (12) proceeded smoothly to yield
N-phenylmorpholine (13) in good yield (entry 5).

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Table 1. Base-mediated benzyne generation from 2-(trimethylsilyl)phenyl triflate (1a).
10133
Entry
1
Activator
Cs2CO3
Cs2CO3
Cs2CO3
Cs2CO3
Cs2CO3
Cs2CO3
Cs2CO3
Cs2CO3
Cs2CO3
CsHCO3
K2CO3
K2CO3
K3PO4
KF
Additive
–––
Solvent
THF
Temp. (°C)
Yield (%) a
25
60
25
60
25
25
25
25
25
25
25
25
25
25
1
32
2
–––
THF
3
–––
MeCN
MeCN
THF
38
4
–––
79
5
18-crown-6
18-crown-6
18-crown-6
18-crown-6
18-crown-6
18-crown-6
18-crown-6
18-crown-6
18-crown-6
18-crown-6
–––
88 (86) b
72
6
MeCN
CH2Cl2
toluene
DME
THF
7
13
8
59
9
88
10
11
12 c
13
14
15
0
THF
37
THF
76
THF
37
THF
99
CsF
MeCN
25
quant.
a
b
Yields determined by 1H-NMR analyses unless otherwise noted;
c 4.0 equivalents of 18-crown-6 were used.
Isolated yield in parentheses;
Table 2. Reactions of benzyne generated from 1a with various arynophiles.
Entry
Arynophile
Product
Yield (%) a
1
4
6
5a
7
73
2
87
PhN
Ph
N
3
4
8
9
74
84
10
11
5
12
13
75
a Isolated yields.

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The aryne generation method mediated by cesium carbonate and 18-crown-6 was also successfully
applied to generate arynes from various ortho-(trimethylsilyl)aryl triflates, and this was demonstrated in
the reaction with 4 (Table 3). Indeed, 3- and 4-methoxybenzynes were generated efficiently from the
corresponding ortho-silylaryl triflates 1b and 1c, respectively, to provide the cycloadducts 5b and 5c in
high yields (entries 1 and 2). Reactions of 3- and 4-methylbenzyne precursors, 1d and 1e, as well as 2,3-
and 1,2-naphthalyne precursors, 1f and 1g, also proceeded smoothly to afford the cycloadducts 5d–g in
high yields (entries 3–6).
Table 3. Cycloaddition of various arynes with furan.
Entry
Arynophile
Product
Yield (%) a
1
1b
1c
1d
5b
5c
5d
89
2
3
86
88
4
5
1e
1f
5e
5f
89
76
6
1g
5g
85
a Isolated yields.
We then turned our attention to the remarkable effect elicited by 18-crown-6-ether, which is able
to retain a potassium ion inside the molecule or alternatively coordinate a cesium ion to form
a sandwich-type complex [39–42]. To examine the effects of the countercations of the bases, and the
ring size of the crown ether, the efficiencies of benzyne generation from ortho-silylphenyl triflate 1a
were compared using several alkali metal carbonates (Na2CO3, K2CO3, Rb2CO3, and Cs2CO3) or
fluorides (NaF, KF, RbF, and CsF) in combination with any one of three crown ethers, 15-crown-5,
18-crown-6, and 24-crown-8, in the presence of benzyl azide (2) (Figure 1A). Consequently, the yield
of benzotriazole 3, which reflects the efficiency of benzyne generation, increased as the size of the alkali
metal cation of the carbonates became larger. For instance, when 15-crown-5 was employed, the order
of the yields of 3 was Na (0%) < K (34%) < Rb (75%) < Cs (86%). A similar trend was observed when

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18-crown-6 or 24-crown-8 was used. Fluoride ion-mediated benzyne generation showed the same
tendency, Na << K < Rb ≈ Cs, although higher yields of 3 were generally obtained compared with those
observed in the carbonate-mediated conditions. These results indicate that the countercation of the base
also plays an important role in activating ortho-silylaryl triflate for benzyne generation. Moreover,
although the use of a crown ether having a hole size smaller than the size of a metal ion (Figure 1B,C)
was prone to increase the efficiency of benzyne generation from 1a, the use of a larger crown ether, such
as 24-crown-8, was less effective, particularly when K2CO3, Rb2CO3, or KF was used as the base.
Figure 1. Generation of benzyne from 1a using various alkali metal carbonates or fluorides
and crown ethers. (A) Efficiency of the reactions between 1a and 2 using various bases in
combination with different crown ethers (N: without crown ethers; 15: with 15-crown-5; 18:
1
with 18-crown-6; 24: with 24-crown-8). Yields determined by H-NMR analyses;
(B) Hole size of crown ethers; (C) Diameter of alkali metal ions.
Various other crown ethers, regardless of their ring size and benzene- or cyclohexane-linked structure,
also effectively supported the cesium carbonate-mediated generation of benzyne from 1a (Figure 2,
entries 1–7). On the other hand, the use of acyclic tetraethylene glycol dimethyl ether or polyethylene

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glycol dimethyl ether (average molecular weight 240) instead of the crown ether drastically decreased
the efficiency (entries 8 and 9). These results suggest that an appropriate complexation between an alkali
metal carbonate and a crown ether, such as between cesium carbonate and 18-crown-6, assists the smooth
liberation of the triflyloxy anion.
Figure 2. Efficiency of the reactions between 1a and 2 using cesium carbonate in combination
with different ethers. Yields determined by 1H-NMR analyses.
3. Experimental Section
3.1. General Remarks
All reactions were performed in dried glassware under an argon atmosphere unless otherwise noted.
All chemical reagents used were commercial grade and used as received. Aryne precursors 1a–1g were
purchased from Tokyo Chemical Industry Co., Ltd. (Tokyo, Japan). Analytical thin-layer
chromatography (TLC) was performed on precoated (0.25 mm) silica-gel plates (Silica Gel 60 F254, Cat.
No. 1.05715, Merck Millipore, Darmstadt, Germany). Column chromatography was conducted using a
ZIP sphere cartridge [silica], 10 g (Cat. No. 445-1000-FZ-20, Biotage®, Uppsala, Sweden), with a
medium pressure liquid chromatograph (W-Prep 2XY A-type Yamazen, Osaka, Japan).
1H-NMR spectra were obtained with an AVANCE 400 spectrometer or an AVANCE 500 spectrometer
13
at 400 or 500 MHz, respectively (Bruker BioSpin K.K., Karlsruhe, Germany). C-NMR spectra were
obtained with a Bruker AVANCE 500 spectrometer at 126 MHz. CDCl3 (Cat. No. 368651000, Acros
1
Organics, Geel, Belgium) was used as a solvent for obtaining NMR spectra. H-NMR yields were

Molecules 2015, 20
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determined using 1,1,2,2-tetrachloroethane as an internal standard. The spectra obtained for products
3 [28], 5a [43], 5b–d [44], 5e [45], 5f [46], 5g [47], 7 [28], 9 [28], 11 [28], and 13 [48] were identical to
those reported in the corresponding references.
3.2. Typical Procedure for Aryne Generation from ortho-Silylaryl Triflate with Cesium Carbonate in
the Presence of 18-Crown-6
To a mixture of 2-(trimethylsilyl)phenyl triflate (1a, 150 mg, 0.503 mmol) and benzyl azide (2, 333 mg,
2.50 mmol) dissolved in tetrahydrofuran (2.5 mL) was added cesium carbonate (326 mg, 1.00 mmol)
and 18-crown-6-ether (265 mg, 1.00 mmol) at room temperature. After stirring for 24 h at 25 °C, water
(10 mL) was added to the mixture. The mixture was then extracted with ethyl acetate (15 mL × 3), and
the combined organic extract was washed with brine (10 mL), dried (Na2SO4), and, after filtration, the
filtrate was concentrated under reduced pressure. The residue was purified by column chromatography
(silica-gel 10 g, n-hexane/EtOAc = 5/1) to give 1-benzyl-1H-benzo[d][1,2,3]triazole (3, 90.0 mg,
0.431 mmol, 85.6%) as a colorless solid.
4. Conclusions
We have demonstrated that cesium carbonate, in the presence of 18-crown-6, triggers the efficient
generation of arynes from ortho-silylaryl triflates under mild conditions. The method was applicable
to a variety of reactions between several arynes and arynophiles. Various crown ethers other than
18-crown-6 were found to be similarly effective, but the efficiency of aryne generation significantly
depended upon the alkali metal countercation of the carbonate. Further studies to demonstrate the
advantage of this newly developed method are underway.
Acknowledgments
The initial concept of this work was conceived by one of the authors (Y.S.) during his short stay as a
visiting student (JSPS Research Fellowships for Young Scientists) during August–October 2009 at the
group of Mark Lautens (Department of Chemistry, University of Toronto, Toronto, ON, Canada), to
whom we express special thanks. This work was supported by the Platform for Drug Discovery,
Informatics, and Structural Life Science from MEXT, Japan; JSPS KAKENHI Grant Numbers
15H03118 (T.H.) and 26350971 (S.Y.); and Azuma Medical & Dental Research Grant (S.Y.).
Author Contributions
Y.H., Y.S., and T.Y. performed the experiments; S.Y. and T.H. designed the experiments and
wrote the paper.
Conflicts of Interest
The authors declare no conflict of interest.

Molecules 2015, 20
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