H-bonded reusable template assisted para-selective ketonisation using soft electrophilic vinyl ethers.

In nature, enzymatic pathways generate Caryl-C(O) bonds in a site-selective fashion. Synthetically, Caryl-C(O) bonds are synthesised in organometallic reactions using prefunctionalized substrate materials. Electrophilic routes are largely limited to electron-rich systems, non-polar medium, and multiple product formations with a limited scope of general application. Herein we disclose a directed para-selective ketonisation technique of arenes, overriding electronic bias and structural congestion, in the presence of a polar protic solvent. The concept of hard-soft interaction along with in situ activation techniques is utilised to suppress the competitive routes. Mechanistic pathways are investigated both experimentally and computationally to establish the hypothesis. Synthetic utility of the protocol is highlighted in formal synthesis of drugs, drug cores, and bioactive molecules.

Introduction

Carbon−Carbon bonds constitute the major backbone of organic molecules. Prudent construction of such linkages facilitates structural manipulation and complex total synthesis.[1] Synthetic methodologies, thriving to transform robust C−H bonds into diverse functional motifs, can potentially shift the retrosynthetic paradigm. Recent exercise on C−H bond functionalization prompted us to sketch a generalised route of site-selective C−C bond formation at a distal para position of an arene, attenuating structural and electronic constraints. Although statistically such transformations are highly probable, inert nature and minimal reactivity distinction impose significant synthetic challenges to target a particular C−H bond. In nature, para-toluene monooxygenase functionalise para C−H bonds of toluene distinctively.[2,3] Although synthetic reproduction of such transformation can be attained for biased substrates, it falters in recapitulating the enzymatic efficiency with unbiased and deactivated substrates.

In biosynthetic pathways, ketoacyl-synthase and benzophenone synthase transfer R−C(O) groups to form C−C(O) connectivity.[4-6] Synthetically carbonyl cores can be accessed using organometallic reagents and cross-coupling at the expense of sensitive reagents and prefunctionalized reactants.[7-13] On the contrary, electrophilic substitutions (Friedel–Crafts acylation) are more atom economical yet biased to electron-rich systems and sensitive to substituents. Electronic effect of the substituents often leads to the inseparable mixtures of isomers whereas it mostly fails with electron-deficient systems. Broadly, the need of non-nucleophilic solvent medium further confines the scope.[14-16] In the present work, we intend to circumvent such limitations both in terms of selectivity as well as reactivity of the reagents. Over the last few decades directed C−H activation has offered a promising strategy for superior regioselectivity.[17-39] However, directed carbonyl insertion is mostly explored for ortho C−H bonds.[40-44] Expanding the idea to distal para positions, spans larger separation and thus tunnels through bulky and strained intermediates, vulnerable to subtle manifold modification.[45-49]

Comprehending the significance of carbonyl scaffold[50] and synthetic challenges, herein we disclose directed para-selective ketonisation of arenes by overriding the electronic bias, in the presence of a polar solvent (Fig. 1).

Fig. 1

Overview of the work. a Diverse functions of ketones. b Classic synthetic routes for ketone synthesis and its drawbacks. c Mechanistic hypothesis for generalised approach and key outline of the work

Results

Design of template and optimisation

Initially acylation reaction was chosen as the prototype transformation with a toluene model substrate, appended with the first-generation biphenyl nitrile directing template (Fig. 2). A series of different acylating agents were screened. Interestingly, the usage of protic solvent under elevated temperature consumed electrophilic acid chlorides and anhydrides. Therefore, selection of a compatible acylating agent was imperative. In view of competitive nucleophilicity of the solvent and metallacycle, we envisioned to identify a soft masked acylating agent to facilitate interaction with soft metallacycles (Fig. 2). In this regard, first breakthrough was obtained with ethyl vinyl ether in the presence of catalytic Pd(OAc)2 and hexafluoroisopropanol (HFIP) solvent with an overall yield of 11% and 2:1 para-selectivity. Notably, vinyl ethers are electron rich and less reactive and thus less pronounced as cross-coupling partner.[51-66] Additionally, the possibility of linear and branched isomer formation along with an additional hydrolysis step to release the carbonyl unit is noteworthy.[67] However, in stark contrast, vinyl ether worked satisfactorily under the current condition in a one-pot process. To seek better selectivity and yield different directing groups were tested. Replacement of the linear nitrile group by heterocyclic metal coordinating motifs such as pyridine (DG), pyrimidine (DG), and methoxy quinoline systems (DG) improved yield yet compromised the selectivity. Apparently, methoxy quinoline (DG7), due to its increased bulk, destabilises the necessary orientation by pushing the toluene nucleus away exposing the meta-C–H bond for reaction. In stark contrast, alteration of the electronic environment of the nitrile-based directing group (DG, DG, and DG) offered significant improvement both in yield and selectivity. A yield of 52% with 11:1 para-selectivity was obtained with a second-generation hydrogen-bonded para-directing template (DG). In particular, the presence of two methoxy groups triggered facile metal-CN binding offering better yield, whereas template-solvent H-bonding interaction generated optimum rigidity to ensure superior selectivity.[46] Under optimised condition Pd(OAc)2 along with N-Cbz-Gly gave 80% yield and 16:1 para-selectivity in the presence of NaOAc and Ag2CO3. Control experiment with a simple toluene substrate under the optimised reaction condition gave a mixture of products with no signature of desired para-acylated product formation.[68] Such a phenomenon clearly indicates the significant role of the directing template in selective para functionalization.

Fig. 2

Development of para-ketonisation reaction. a Significance of the directing group. b Screening of the reaction parameters

Scope of the methodology

Once optimised, the scope of vinyl ether was tested (Table 1). Both cyclic and acyclic alkenyl ethers offered good yield (1a–1c, 1g, 1h, and 1k). No competitive product formation was observed for allyl vinyl ether, divinyl polyether, and free −OH group (1d, 1i, 1j, and 1l). Interestingly, vinyl silane and vinyl borane were found to be compatible (1e and 1f). A number of substituents both aliphatic and aromatic moieties around the vinyl group were tested successfully. Both electron-rich and -deficient arene rings were tolerated under the standard condition (1u–1r and 1w–1z). Di-substitution vinyl ether led to the formation of corresponding α−di (1z) substituted ketonised product.

Table 1

The scope of vinyl ether

para: others selectivity for entries 1a–1p is 16:1; yields in parenthesis are based on the recovered starting material.

Following the diversification on alkoxy and vinyl substituents, the scope of arenes was explored (Tables 2–4). With electron-rich systems (Tables 2; 2a–2i) a predictable para-selectivity was obtained by virtue of the directing group. Despite the possibility of random electrophilic functionalization, para-ketonised product was obtained in synthetically useful yield and selectivity. However, ortho-trifluoromethoxy toluene (2d) offered a moderate selectivity as compared to methyl (2b) substituent. Although the reason of such an anomaly is unclear, it is worth mentioning that −OCF3 can influence the outcome of a transformation not just by electronic effect but also distorting the planer alignment with the benzene ring which can have a significant impact on the transformation, relied on the appropriate spatial orientation.[69,70] Nevertheless, the current methodology complemented the electrophilic route with excellent para-selectivity.

Table 2

The scope of electron-rich arenes

Table 4

Scope of arenes

aN-Ac-Gly used as ligand

Although electron-deficient systems are not susceptible towards electrophilic substitution reaction, para-ketonisation generated the desired product with excellent yield and selectivity (Table 3: 3a–3k). Poly-halo compounds, specially poly-fluoro, which is having significant medicinal values can be functionalized using the current protocol. Notably, comparable results for both the electron-rich and electron-deficient arenes re-establish the prominent influence of the directing template over other paraphernalia.

Table 3

Scope with electron-deficient arenes

Arenes with both electron-rich and electron-deficient substituents were also found to be compatible (Table 4). T4 template played the key role to dictate the selectivity. Substrates with benzylic substitution (4k–4m) underwent mono para-acylation successfully (4m).

Experimental mechanistic evidences

Following the scope of the reaction, a series of control experiments were conducted to gain better insight of the mechanism (Fig. 3). As the vinyl moiety of ether rearranges to the carbonyl group, we were intrigued to understand the stepwise pathway. NMR titration showed a slow hydrolysis of vinyl ether in the presence of HFIP, generating multiple products including aldehyde which was accelerated upon heating. The control experiment revealed that the hydrolysed product is ineffective as the acylation agent. Upon replacement HFIP by d2-HFIP or isopropanol, less acidic variant of HFIP, neither decomposition nor the desired product formation was observed. Seemingly, the protonation of the ether by HFIP is responsible for the generation of the reactive intermediate of ketonisation.

Fig. 3

Influence of HFIP. a Control experiment for vinyl ether–HFIP interaction. b NMR study of vinyl ether–HFIP interaction

During the scope of the reaction thiovinyl ether, unlike vinyl ether, failed completely (Fig. 4a) to deliver the desired carbonyl product which further strengthens the hypothesis of protonation by HFIP. Once insertion into the palladacycle, vinyl ether can undergo either nucleophilic pathway (P1) or elimination pathway (P2) of hydrolysis to generate the target molecule. The possibility of both hydrolytic pathways can be rationalised from the reactivity of different alkoxy substituted vinyl ethers (Fig. 4a). Product distribution and kinetic isotope effect study of the deuterated substrates (kH/kD = 3.1; PH/PD = 3.4) revealed C−H activation as the rate-limiting step (Fig. 4b).[69]

Fig. 4

Understanding the mechanistic features. a Plausible pathways of hydrolysis. b Determination of kinetic isotope effect (KIE)

DFT calculations and mechanistic cycle

Based on these mechanistic experiments, a plausible catalytic cycle for para-ketonisation was proposed (Fig. 5b). The pathway was evaluated by density functional theory calculations (Fig. 5a). Initial steps of the para-selective ketonisation was found to resemble para-selective C–H silylation of 1.[46] Compared to para-C–H palladation, meta-C–H palladation is disfavoured due to greater ring strain and distortion of the 15-membered palladacycle in the transition state.[46,68] The para-C–H metalation occurs via the CMD mechanism directed by the Si-based T4-directing group to form palladacycle 5. Subsequent olefin migratory insertion (TS1) requires a relatively low activation free energy of 16.0 kcal/mol. The β-elimination of the benzylic hydrogen (TS2) is facile, requiring only 10.4 kcal/mol, to form the Pd hydride species 8, which upon reductive elimination yields the alkenyl ether product 9. Finally, hydrolysis of alkenyl ether 9 leads to the desired product formation via pathway P1 or P2. It is noteworthy that apart from generating the activated vinyl ether, HFIP solvent molecule forms H-bonding with the methoxy group of the template (T4) which favours the bent geometry of C–H metalation transition state, thus metal binding and improved para selectivity.[46]

Fig. 5

Stepwise mechanism of para-ketonisation. a Energy profile of the para-C−H acylation with vinyl methyl ether. Energies are with respect to the palladacycle 5. See SI for the complete energy profile. Method: M06/SDD-6-311 + G(d,p)/ SMD(HFIP)//B3LYP/SDD-6-31G(d). b Plausible catalytic cycle

Template recovery and applications

During para-ketonisation, the presence of the template (T4) was essential for improved selectivity and yield, yet its removal is required for further synthetic applications (Fig. 6). Almost a quantitative amount of directing was recovered from the 1q (96%) along with the formation of (p-tolyl)-1-propanone (5b) which was further used for α- functionalization and cyclization. Recovery of T4 from 4m led to the formation of mono ketonised benzhydryl cores (5a).[68]

Fig. 6

Synthetic utilities of para-ketonisation. a Selective mono ketonisation of benzhydryl core. b Applicative highlights of the methodology

Discussion

Therefore, we have developed a reusable template-assisted para-selective ketonisation of toluene derivatives with vinyl ethers in the presence of polar protic HFIP. The protocol allows a broad spectrum of vinyl ether and arenes. Also, it can withstand electron deficiency and steric congestion, which is likely to diminish reactivity significantly. The sequence of activation, insertion, and hydrolysis was experimentally investigated and was further supported by computational studies.

Methods

Procedure of para-ketonisation

In an oven-dried screw-capped reaction tube was charged with a magnetic stir-bar, benzylsilyl ether substrate (viscous benzylsilyl ether was weighed first), Pd(OAc)2 (10 mol%), ligand (N-CBZ-Gly or N-Ac-Gly; 20 mol%), Ag2CO3 (3 eq.) and NaOAc (2 eq.). About 1.2 mL (for 0.1 mmol scale) of 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) was added followed by vinyl ether (3 eq.). The reaction tube was capped and stirred (900 rpm) on a preheated oil-bath at 80 °C for 24/36 h. Upon completion the mixture was cooled and diluted with EtOAc and filtered through a celite pad. The filtrate was evaporated under reduced pressure and the crude mixture was purified by column chromatography using silica (100–200 mesh size) and petroleum ether/ethyl acetate as the eluent. The selectivity was monitored using 1H-NMR signal in the presence of 1,3,5-trimethoxybenzene as an internal standard. The regioselectivity was determined from 1H-NMR signals of aromatic region and benzylic position.

In the substrate scope table, selectivity was obtained from 1H-NMR.

Supplementary Data 1

Peer Review File

Supplementary Data 2