Iridium-Catalyzed α-Selective Arylation of Styrenes by Dual C-H Functionalization.

An IrI -system modified with a ferrocene derived bisphosphine ligand promotes α-selective arylation of styrenes by dual C-H functionalization. These studies offer a regioisomeric alternative to the Pd-catalyzed Fujiwara-Moritani reaction.

The intermolecular Heck reaction is the foremost method available for the C−H arylation of alkenes.1 For processes involving styrenes, arylation occurs predominantly at the β‐position.1, 2 In electronically predisposed cases, significant levels of α‐arylation are observed,3 but complete selectivity for C−C bond formation at this position can be achieved only under specialized conditions.4 The related intermolecular Fujiwara–Moritani reaction, which is most effective in the presence of directing groups, operates under oxidative conditions and is attractive because it achieves C−H arylation of alkenes by dual C−H functionalization, thereby circumventing the preparation of an aryl (pseudo)halide (Scheme 1 A).1c, 5 The regioselectivity trends of this process mirror the Heck reaction, such that the method also does not provide a general approach to the α‐selective arylation of styrenes. This type of selectivity has been observed in rare cases involving heteroarenes, but substrate scope is severely limited.6 The paucity of general methods for direct styrene α‐arylation often mandates multistep synthetic workarounds, thereby increasing cost, effort, and waste.7

Scheme 1

Introduction.

We have previously described Ir‐catalyzed branch selective hydroarylations of styrenes with acetanilides 1 (DG=NHAc, Scheme 1 B).8a These processes were posited to occur via a sequence of carbonyl directed C−H activation (to I), alkene hydrometallation (to II), and C−C reductive elimination (to 3). In this report, we show that modification of the Ir‐center with specific bisphosphine ligands alters the reaction outcome to provide a method for the α‐selective arylation of styrenes (1 to 4). This new dual C−H functionalization method is regioisomeric with respect to the Fujiwara–Moritani and Heck reactions,1, 5 and previous Ir‐catalyzed C−H alkenylation processes,9, 10 thereby providing proof‐of‐concept for a unique approach to the α‐arylation of styrenes. Note that products mechanistically related to 4 have been observed as minor components in enamide C−H alkylation reactions.11

Natural abundance 13C kinetic isotope effect (KIE) experiments on our previously developed alkene hydroarylation reaction (1 to 3, DG=NHAc) are suggestive of a C−C reductive elimination pathway for the formation of 3 (see the Supporting Information).8a,8b, 12, 13 Accordingly, we reasoned that the proposed C−H alkenylation process outlined in Scheme 1 B (1 to 4) requires a catalyst system that can enforce access to an alkene carbometallation manifold at the expense of the prevailing C−C reductive elimination pathway. It has previously been shown by Shibata and co‐workers that styrene carbometallation occurs with complete branch selectivity using bisphosphine‐ligated iridacycles derived from C−C bond activation of biphenylene.14 Accordingly, if a carbometallative manifold could be accessed, then we expected high regioselectivity for the formation of III, which, in turn, would provide α‐arylated styrene 4, rather than the corresponding β‐arylated isomer (not depicted).

An assay of potential ligand systems was undertaken on the coupling of acetanilide 1 a and styrene 2 a using [Ir(cod)2]OTf as precatalyst and dioxane as solvent. From these studies, we observed that the use of dppf (L‐1) afforded a 3:7 mixture of alkene 4 aa and hydroarylation product 3 aa, with the former generated in 23 % yield. This prompted the evaluation of a variety of related ligand systems L2–L6, which were prepared in three steps from ferrocene (see the SI).15 In general, the selectivity for alkenylation vs. hydroarylation, and the yield of 4 aa increased as the aromatic unit of the ligand became more electron poor, with L‐4 providing 4 aa in 24 % yield and 8:2 selectivity over 3 aa. However, L‐5, which possesses highly electron withdrawing pentafluorophenyl units, did not provide 4 aa, and instead a mixture of branched and linear hydroarylation products 3 aa and ‐3 aa formed.16 Ligand systems with more electron rich aromatic units, such as L‐6, were not effective, and resulted in hydroarylation only. As L‐4 provided the highest selectivity for 4 aa, further optimization studies were undertaken using this ligand. Pleasingly, by increasing the reaction time to 72 hours we found that 4 aa could be formed in 62 % yield. The conversion of III to 4 releases an IrIII‐dihydride, and, as indicated by GCMS analysis of crude reaction mixtures, turnover is achieved by reduction of a sacrificial equivalent of styrene to ethyl benzene. As such, we reasoned that oxidants other than styrene might offer additional improvements. In the event, by using 200 mol % tert‐butylethylene as an exogenous oxidant9 and increasing the catalyst loading to 7.5 mol %, 4 aa was formed with 10:2 selectivity over 3 aa and could be isolated in pure form in 74 % yield (further optimization studies with respect to the oxidant are detailed in the SI). For clarity, the product numbering system used in Table 1 is retained throughout subsequent discussion: 3=hydroarylation product; 4=C−H arylation product; first letter specifies anilide precursor; second letter specifies styrene precursor.

Table 1

Selected optimization results.

[a] Yields and selectivities were determined by 1H NMR analysis using 1,3,5‐trimethoxybenzene as a standard. [b] Reaction run at 0.5 M. [c] Isolated yield.

With optimized conditions in hand, we sought initially to explore scope with respect to the directing group (R1, Table 2 A). These studies revealed that a wide range of sterically distinct anilide‐based systems can be employed (1 a–i), such that 4 aa–ia were all formed in good to excellent yield, with high selectivity over the corresponding hydroarylation product (3).17 Note that systems where R1=aryl are not suitable because competing ortho‐ selective hydroarylation of this unit predominates.8c The process tolerates diverse substitution on the anilide partner (Table 2 B). Indeed, para‐substituted systems engage efficiently (4 oa–rb), and arenes possessing meta‐substitution undergo highly regioselective C−H alkenylation at the less hindered ortho‐position; for example, C−H arylation of styrene 2 a with acetanilide 1 m provided 4 ma (65 % yield) as a single regioisomer and with good selectivity over the corresponding hydroarylation product (5:1). The functional group compatibility of the process is good, with, for example, the potentially labile C−Br bond of 4 oa remaining intact for further diversification. Ortho‐substitution can impact selectivity; 4 ua was formed with only 2:1 selectivity over 3 ua, but generation of 4 vb was highly selective. In all cases, the target products were easily separated from the minor hydroarylation products by column chromatography.

Table 2

Scope of the anilide component.[a]

[a] Isolated yields of the C−H arylation product are quoted. Selectivites (C−H arylation product 4: hydroarylation product 3) were determined by 1H NMR analysis of crude material and are quoted in parentheses. [b] 10 mol % catalyst was used.

Using anilide 1 f, we have assessed the scope of the alkenylation process with respect to the styrene partner (Table 3). Electronically diverse systems all participate with acceptable levels of efficiency; for example, para‐fluoro system 4 fd and para‐methyl system 4 fb were generated in 75 % and 77 % yield, respectively. An electronic trend is evident for alkenylation vs. hydroarylation selectivity (cf. 4 fb vs. 4 fe), however, steric effects are more pronounced. Indeed, ortho‐substitution on the styrene lowers product selectivity, such that fluoro system 4 fj was formed with 2:1 selectivity over the corresponding hydroarylation product. Despite this modest selectivity, analytically pure 4 fj could still be isolated in 50 % yield. At the present stage, the process is applicable to styrenes only; alkyl substituted alkenes participate with low levels of efficiency with respect to both yield and product selectivity.

Table 3

Scope of the styrene.[a]

[a] See Table 2 footnotes. [b] 10 mol % catalyst was used. [c] Run at 1.0 M.

The anilide‐based C−H alkenylation products are useful intermediates for synthesis, especially in heterocyclization processes. Treatment of the alkenylation products with POCl3 effects smooth cycloaromatization to provide quinolines,18 as exemplified by the synthesis of 5 a–d (Scheme 2 A). Note that this de novo heteroaromatization strategy offers high levels of modularity, and its suitability for the construction of challenging polycyclic systems, such as 5 c and 5 d, is significant. The protocol even extended to the two‐step conversion of estrone derived acetanilide 1 w to the unusual quinoidal steroid 5 e. Other classes of heterocyclization can also be achieved; treatment of 4 aa with SelectFluor19 or iodine20 provided adducts 6 and 7, respectively (Scheme 2 B). Free aniline 8 was accessed by acid hydrolysis of 4 ha and could be converted in high yield to cinnoline 9 or dihydroquinoline 10, which possesses a tetrasubstituted stereocenter.

Scheme 2

Product derivatizations.

The C−H alkenylation processes outlined here represent proof‐of‐concept for a broader family of styrene α‐arylation protocols. In preliminary efforts to extend the scope of our approach, we have assayed a selection of other aromatic partners leading to the observation that α‐selective arylation using pyrrole 11 a is feasible (Scheme 3 A). Here, L‐4 was not a suitable ligand, but, instead, we found that use of ferrocene‐based system (S,S)‐f‐Binaphane21 provided targets 12 a–c in 62–74 % yield. The seemingly fickle nature of the ligand requirements highlights a future challenge in the development of new processes. For pyrrole 11 b, which is arylated at C3, C−H alkenylation to provide 12 d was highly regioselective. Using L‐4 we have also found that dehydrogenative C−C bond formation can be combined with a further dehydrogenation event. When enamide 13 was exposed to optimized conditions dehydrogenative aromatization (to 1 n) was followed by C−H alkenylation, which provided 4 na in 60 % yield (Scheme 3 B).22

Scheme 3

Extensions of the C−H alkenylation process.

It is pertinent to comment on mechanistic details of the processes described here. A control experiment involving resubjection of hydroarylation product 3 aa to optimized C−H arylation conditions did not provide alkene 4 aa. This result supports the idea that 4 aa is generated via a carbometallative pathway (I to III to 4 in Scheme 1 B) rather than via dehydrogenation of 3 aa. C−H arylation of deuterio‐2 c with acetanilide 1 q resulted in scrambling of the deuterium labels in product deuterio‐4 qc and in recovered deuterio‐2 c and 1 q. This suggests that reversible styrene hydrometallation (I to II) is also operative under optimized conditions (Scheme 4). Accordingly, the minor alkene hydroarylation products (e.g., 3 aa) might arise via either C−C reductive elimination from II or C−H reductive elimination from III. At the present stage we have been unable to discriminate these pathways, such that meaningful rationalizations for product selectivity in each case cannot be made.

Scheme 4

A deuterium labelling study.

In summary, we outline a unique Ir‐catalyzed method for the α‐selective C−H arylation of styrenes. This dual C−H functionalization protocol offers a regioisomeric alternative to the well‐established Pd‐catalyzed Fujiwara–Moritani reaction. Efforts to broaden the utility of the method are ongoing and the results of these studies will be reported in due course.

X‐ray data is available under CCDC 1838966–1838967.

Conflict of interest

The authors declare no conflict of interest.

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Supplementary

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