Wei
Ding
a,
Chen
Wang
ab,
Jie Ren
Tan
a,
Chang Chin
Ho
a,
Felix
León
a,
Felipe
García
*a and
Naohiko
Yoshikai
*a
aDivision of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore. E-mail: fgarcia@ntu.edu.sg; nyoshikai@ntu.edu.sg
bZhejiang Key Laboratory of Alternative Technologies for Fine Chemicals Process, Shaoxing University, Shaoxing 312000, China
First published on 23rd June 2020
An efficient and site-selective aromatic C–H λ3-iodanation reaction is achieved using benziodoxole triflate (BXT) as an electrophile under room temperature conditions. The reaction tolerates a variety of electron-rich arenes and heteroarenes to afford the corresponding arylbenziodoxoles in moderate to good yields. The reaction can also be performed mechanochemically by grinding a mixture of solid arenes and BXT under solvent-free conditions. The arylbenziodoxoles can be used for various C–C and C–heteroatom bond formations, and are also amenable to further modification by electrophilic halogenation. DFT calculations suggested that the present reaction proceeds via a concerted λ3-iodanation–deprotonation transition state, where the triflate anion acts as an internal base.
Trivalent iodine (λ3-iodane) moieties represent a class of useful nucleofuges in arene transformations. Thus, vast arrays of aryl–carbon and aryl–heteroatom bond forming reactions have been developed using diaryliodonium salts as electrophilic aryl-transfer agents.5 Particularly attractive among diaryliodonium salts are the unsymmetrical ones that allow selective transfer of one of the aryl groups over the other, “dummy” aryl group (e.g., mesityl).6,7 A direct C–H λ3-iodanation approach has proved feasible for the synthesis of such compounds from electron-rich (hetero)arenes and bulky aryl-λ3-iodane reagents such as MesI(OH)OTs with an acidic activator, or from (hetero)arenes, bulky aryl iodide, oxidants and acids.8 However, diaryliodonium salts are potentially unstable for isolation and prolonged storage and are often used without isolation.8a–c In this context, aryl-λ3-iodane compounds bearing a cyclic benziodoxol(on)e (BX) moiety could be a valuable alternative or complement to diaryliodonium salts, as their non-ionic nature and rigid structure would endow them with enhanced stability for facile isolation and long-term storage as well as the ability to tolerate a wider range of reaction conditions. The BX group has already played an important role in the development of reagents for transferring groups such as trifluoromethyl, alkynyl, azido, and cyano groups.9 On the other hand, access to analogous (hetero)aryl–BX reagents remains relatively limited and their reactivity less explored. The direct preparation of aryl–BXs from arenes and 2-iodobenzoic acid was reported by Olofsson and Zhdankin (Scheme 1a).10 However, these compounds have not been utilized as aryl transfer agents. Instead, they were reported to produce 2-functionalized benzoic acids in the reaction with nucleophiles.10b More recently, Waser developed indole- and pyrrole-BX reagents via zinc-catalyzed BX transfer to indoles and pyrroles with acetoxy benziodoxolone and demonstrated their utility in C–H functionalization reactions (Scheme 1b),11,12 while the reaction required relatively high dilution and was not extended to arenes.
Herein, we report that Zhdankin's benziodoxole triflate (BXT; 1) derived from α,α-bis(trifluoromethyl)-2-iodobenzyl alcohol13 facilitates C–H λ3-iodanation of (hetero)arenes with high site selectivity (Scheme 1c). This BX transfer reaction tolerates various electron-rich arenes and heteroarenes, allowing facile preparation of the corresponding aryl–BX derivatives in moderate to excellent yields under simple and mild conditions without any catalyst or promoter. Moreover, the reaction can also be performed mechanochemically using solid arenes and BXT under solvent-free conditions. The aryl–BX compounds serve as aryl donors for a variety of C–C and C–heteroatom bond formations, and also tolerate further modification by electrophilic halogenation. Owing to the superior leaving group ability of the BX group, iodinated aryl–BX compounds can be used for chemoselective sequential cross-couplings.
Entry | Solvent | Yieldb (%) |
---|---|---|
a Unless otherwise noted, the reaction of 1 (0.10 mmol) and 2a (0.15 mmol) was carried out in the solvent (0.25 mL) at room temperature. b Determined by 19F NMR using 1,4-bis(trifluoromethyl)benzene as an internal standard. c 1 (0.10 mmol) and 2a (0.10 mmol) were used. d 1 (0.20 mmol) and 2a (0.10 mmol) were used. | ||
1 | MeCN | 94 |
2 | CH2Cl2 | 83 |
3 | Toluene | 65 |
4 | Chlorobenzene | 69 |
5 | DMF | 0 |
6 | Et2O | 0 |
7 | MeOH | 0 |
8c | MeCN | 84 |
9d | MeCN | 86 |
With the optimized reaction conditions in hand, we explored the scope of the λ3-iodanation reaction (Table 2). A variety of monoalkoxyarenes took part in the reaction to afford the desired aryl–BX products 3a–3e in high yields with exclusive para-selectivity. 1,3-Disubstituted arenes such as m-xylene, resorcinol dimethyl ether, and 3-methoxytoluene regioselectively afforded aryl–BX products 3f–3h with a 1,2,4-substitution pattern. The latter reacted exclusively at the para-position of the methoxy group. 1-Alkoxy-2-substituted benzene derivatives, including dihydrobenzofuran and 9,9-dimethylxanthene, were functionalized at the para-position of the alkoxy group, thus affording the products 3i–3o in moderate to good yields, while elevated temperatures (60–80 °C) were necessary for 1-methoxy-2-halobenzenes. 3-Methylbenzoxazol-2(3H)-one reacted exclusively at the para-position of the nitrogen atom, as unambiguously supported by X-ray crystallographic analysis of product 3p.16 Electron-rich 1,3,5-trisubstituted arenes such as mesitylene, 1-bromo-3,5-dimethoxybenzene, 3,5-dimethylanisole, and N-methyl metaxalone17 took part in the reaction to afford the products 3q–3t in good yields, where, for the latter three, the para-position of the alkoxy group was selectively functionalized. Other trisubstituted methoxyarenes with different substitution patterns were also amenable to the present λ3-iodanation (see the products 3u–3w). Electron-rich heteroarenes such as thiophene and indole derivatives could be employed as substrates for the present reaction, producing the products 3x–3aa in good yields. The scalability of the present λ3-iodanation reaction was demonstrated by gram-scale (3 mmol) synthesis of 3a and 3q, which could be achieved without a significant decrease in the yield (86% and 77% yields, respectively). It should be noted that the present method allows access to unique aryl–BX compounds such as 3m and 3z that contain iodonium and iodide moieties, which would offer opportunities for selective and sequential functionalizations (vide infra).
a The reaction was performed on a 0.2 mmol scale according to the standard conditions described in Table 1, entry 1. BX in the product formula refers to the benziodoxole moiety. b The yield for a 3 mmol-scale reaction is given in the parentheses. c The reaction was performed at 60 °C. d The reaction was performed at 80 °C. |
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Besides arenes and heteroarenes, 1,1-diphenylethene (2ab) and its para-fluoro-substituted derivative (2ac) reacted with BXT under the standard conditions to afford the corresponding alkenyl–BXs 3ab and 3ac in good yields (Scheme 2a).14c–e,18 The reaction of 1,1-di(p-tolyl)ethene (2ac) did not take place under the standard conditions but resulted in the decomposition of 1, while the addition of Na2CO3 and the use of chlorobenzene as the solvent allowed us to obtain the desired product 3ad in a moderate yield (Scheme 2b). Other alkenes such as styrene, α-methylstyrene, and vinylcyclohexane failed to participate in the present C–H λ3-iodanation.
Recently, mechanochemistry has emerged as a powerful tool in synthetic chemistry due to its attractive merits such as a solvent-free process, reduced reaction times, ability to engage poorly soluble solid compounds, and unique reactivity and selectivity.19 Notably, mechanochemistry has proved to offer an ideal means to accelerate the present λ3-iodanation under solvent-free conditions. Thus, by simply subjecting a mixture of an arene (0.3 mmol) and 1 (0.2 mmol) to ball milling (30 Hz for 2 h), aryl–BX derivatives 3o, 3q, 3r, and 3u were obtained in good yields (Scheme 3a). Note that, except for 3q, the starting arenes of these aryl–BXs are solid compounds. Additionally, the mechanochemical synthesis of 3r could be performed on a gram scale using a slight excess of the arene 2r, yielding an analytically pure product without chromatographic purification (Scheme 3b).
Some important limitations of the present λ3-iodanation should be noted. Less electron-rich, electron-neutral or electron-poor arenes did not participate well in the reaction with 1 even at elevated temperatures (up to 80 °C), and were largely recovered. However, the reaction of moderately electron-rich o-xylene, which was sluggish under the original conditions (28% yield at 60 °C), could be promoted by the addition of a Sc(OTf)3 catalyst (20 mol%) and the use of CH2Cl2 as the solvent to afford the corresponding aryl–BX product 3ae in 55% yield (Scheme 4a). Meanwhile, aryl–BXs bearing an electron-neutral phenyl (3af) or electron-deficient 4-bromophenyl (3ag) or 4-cyanophenyl (3ah) group could be synthesized in good yield via silicon-to-iodine(III) or boron-to-iodine(III) aryl transfer20,21 using the corresponding aryltrimethylsilane or aryltrifluoroborate (Scheme 4b and c). Highly electron-rich arenes, such as 1,2- and 1,4-dimethoxybenzenes and N,N-dimethylaniline, failed to give the desired aryl–BX products with 1 and decomposed to α,α-bis(trifluoromethyl)-2-iodobenzyl alcohol. This reduction of the I(III) reagent is likely caused by the ability of these electron-rich arenes to undergo single electron transfer.
Scheme 4 Preparation of aryl–BXs via Lewis acid-catalyzed C–H λ3-iodanation or aryl transfer from aryl silicon or boron reagents. |
The functionalized aryl–BX products obtained by the present reaction could be used as versatile building blocks for further transformations via selective transfer of the arene-derived aryl groups (Scheme 5). As illustrated in Scheme 5a, the benziodoxole moiety in 3a and 3q served as an excellent leaving group in Pd-catalyzed Suzuki–Miyaura, Sonogashira, and Stille couplings, and Miyaura borylation,22 which afforded biaryl 4, aryl alkyne 5, styrene 6, and aryl boronate 7, respectively, in good yields. In addition, aryl–BX 3a was amenable to Cu-catalyzed sulfonylation23 and cyanation,24 affording the corresponding aryl sulfone 8 and aryl nitrile 9, respectively. 3-Iodo-4-methoxyphenyl–BX 3m and 5-iodothien-2-yl–BX 3z underwent site-selective Sonogashira coupling with trimethylsilylacetylene on the aryl–BX moiety over the aryl–iodide moiety to afford the monoalkynylated products 10 and 12, respectively, which illustrated the superior leaving group ability of the BX group in oxidative addition to Pd(0) (Scheme 5b). Subsequent Sonogashira coupling of 10 and 12 with phenylacetylene provided unsymmetrically dialkynylated arenes 11 and 13, respectively. Finally, the compounds 3g and 3o could be regioselectively brominated or chlorinated without affecting the BX group to afford the products 3v, 14, and 15 in good yields (Scheme 5c).3e The sequential installation of BX and halogens may offer a means for chemoselective difunctionalization of aromatic compounds.
To gain insight into the mechanism of the C–H λ3-iodanation, DFT calculations on the reaction between 1 and anisole (2a) were performed (Fig. 1; see the ESI† for the computational details). Prior to the iodanation event, the triflate in 1 slipped to the trans position of the aryl group (1 to 1′viaTS1), which allows 2a to bind to the cis position of the aryl ligand (CP1).25 This is followed by a six-centered TS for concerted λ3-iodanation/deprotonation of the para-position (TS2p, ΔG‡ = 19.3 kcal mol−1) to give the product 3a and TfOH, which is reminiscent of the concerted metalation–deprotonation mechanism in aromatic C–H activation by transition metal carboxylates.25,26 Note that λ3-iodanation without prior isomerization of 1 requires an unreasonably high activation energy (37.3 kcal mol−1; Fig. S4†). The calculated endergonicity (2.1 kcal mol−1) might be a reflection of a computational artifact, which does not take the interaction between TfOH and MeCN (in the solution-phase reaction) or the intermolecular hydrogen bonding between TfOH molecules (in the solid-phase reaction) into account. Consistent with the experiment, analogous transition states for the λ3-iodanation of the ortho- and meta-positions were found to require higher activation energies (20.5 kcal mol−1 and 27.5 kcal mol−1, respectively; Fig. S5†).
Fig. 1 Gibbs free energy diagram for the para C–H λ3-iodanation of anisole (2a) with BXT (1). The bond distances are in Å. |
Footnote |
† Electronic supplementary information (ESI) available. CCDC 1981452. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/d0sc02737e |
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