Yan Caoa,
Somayeh Soleimani-Amiri
*b,
Roya Ahmadi
c,
Alibek Issakhovde,
Abdol Ghaffar Ebadi
f and
Esmail Vessally
g
aSchool of Mechatronic Engineering, Xi'an Technological University, Xi'an, 710021, China
bDepartment of Chemistry, Karaj Branch, Islamic Azad University, Karaj, Iran. E-mail: s.soleimani@kiau.ac.ir
cDepartment of Chemistry, College of Basic Sciences, Yadegar-e-Imam Khomeini (RAH) Shahre Rey Branch, Islamic Azad University, Tehran, Iran
dDepartment of Mathematical and Computer Modelling, al-Farabi Kazakh National University, 050040, Almaty, Kazakhstan
eDepartment of Mathematics and Cybernetics, Kazakh British Technical University, 050000, Almaty, Kazakhstan
fDepartment of Agriculture, Jouybar Branch, Islamic Azad University, Jouybar, Iran
gDepartment of Chemistry, Payame Noor University, P.O. Box 19395-3697, Tehran, Iran
First published on 1st October 2021
Among the wide variety of synthetic transformations of inexpensive and abundant feedstock alkenes, vicinal difunctionalization of carbon–carbon double bonds represent one of the most powerful and effective strategies for the introduction of two distinct functional groups into target compounds in a one-pot process. In this context, the direct alkoxysulfenylation of alkenes has emerged as an elegant method to construct valuable β-alkoxy sulfides in an atom- and pot-economic manner utilizing readily accessible starting materials. Here, we review the available literature on this appealing research topic by hoping that it will be beneficial for eliciting further research and thinking in this domain.
Scheme 2 I2-catalyzed alkoxylative sulfenylation of alkenes 1 with sulfonyl hydrazides 2 and alcohols 3. |
Subsequently, Braga and colleagues demonstrated that the same transformation could be achieved by using disulfides as sulfur sources.20 Thus, in the presence of 20 mol% of I2 as a catalyst and 1.0 equiv. of DMSO as an oxidant under microwave irradiation, alkoxysulfenylation of styrene 5 with a small series of aromatic disulfides 6 and aliphatic alcohols 7 furnished the corresponding β-alkoxy sulfides 8 in high yields and regioselectivities (Scheme 3a). Of note, in this reaction alcohols not only were served as substrates but also as solvents. Intriguingly, when disulfides were replaced with diselenides, the respective β-alkoxy selenide products were obtained in fair to excellent yields. The authors proposed a mechanistic course analogous to that of Tian and co-workers for the alkoxysulfenylation with sulfonyl hydrazides. Recently, Meng and Wang along with their co-workers demonstrated the similar alkoxysulfenylation under visible light irradiation and photocatalyst-free conditions.21 The transformation was performed in DCM at room temperature by using the combination of blue LED and carbon tetrabromide (CBr4). Under these conditions several styrene derivatives 9 carrying various substituents were slowly converted to the corresponding β-alkoxy sulfides 12 in moderate to good yields by treatment with diaryl disulfides 10 and diols 11 (Scheme 3b). The results proved that the lengths of carbon chain in diols had a notable impact on the rate of reaction. Generally, shorter chain diols were found to be more reactive than the longer chain alternatives. The authors attributed this observation to the interaction of the intermolecular hydroxyl groups. It is worth noting that when H2O was used in place of diols under the identical conditions, the hydroxysulfenylated products were obtained in modest to high yields. However, no product was observed when aliphatic alkene or aliphatic disulfide were used as one of the substrates. Furthermore, the process is not viable for gram-scale due to the drastic reduction in the yield (from 69% in the 0.6 mmol scale, to 40% in the 5.0 mmol scale). Several control experiments were implemented to probe the mechanism of this reaction; no reaction was observed in the absence of CBr4 or a light source. Additionally, no reaction could be observed when TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxy) was added to the reaction mixture. On this basis, the authors proposed a plausible mechanistic pathway in which the S–S bond in disulfide 10 undergoes hemolytic cleavage under the irradiation of blue LED to generate thiyl radical A, which after reaction with CBr4 affords a tribromomethyl radical B. Next, abstraction of a hydrogen by the newly formed radical B from diol 11 leads to alkoxyl radical C and HCBr3. Conversely, the addition of another molecule of thiyl radical A to alkene 9 provides carbon-centered radical D. Finally, coupling of alkoxyl radical C with intermediate C gives the desired product 12 (Scheme 4).
In 2015, Fu's research team disclosed the use of easily available 1-(arylthio)pyrrolidine-2,5-diones as an alternative sulfenylating reagent in oxysulfenylation reactions.22 In this investigation, thirty one β-alkoxy sulfides 16 were synthesized in moderate to quantitative yields by direct reaction of various mono-, 1,1-di-, and 1,2-di-substituted alkenes 13 with functionalized 1-(arylthio)pyrrolidine-2,5-diones 14 and aryl/benzyl alcohols 15 in CHCl3 under catalyst- and additive-free conditions (Scheme 5). Noteworthy, in this transformation, the terminal alkenes were more reactive than the internal ones, and aliphatic alkenes were also tolerated, although the products were obtained in lower yields. Regarding the reaction mechanism, the authors proposed the formation of a carbonium ion intermediate A via the reaction of alkene 13 with 1-(arylthio)pyrrolidine-2,5-dione 14 followed by electrophilic attack of the alcohol 15 on the carbocation center (Scheme 6). Recently, Liang and Zhao applied this chemistry in highly enantiselective synthesis of a library of thiolated 1,3-aminoalcohols using a chiral selenide catalyst.23
Scheme 5 Catalyst-free oxysulfenylation of alkenes 13 with 1-(arylthio)pyrrolidine-2,5-diones 14 and alcohols 15. |
Scheme 6 The plausible mechanistic pathway for the reaction in Scheme 5. |
A promising contribution to this field was reported by Yuan, Li, and co-workers in 2015,24 when various terminal aromatic and heteroaromatic alkenes 17 were converted to the corresponding β-alkoxy methyl sulfides 20 through the NH4I-mediated alkoxysulfenylation with dimethyl sulfoxide (DMSO; 18) and alcohols 19 under metal-free conditions. As shown in Scheme 7, this reaction tolerated various primary and secondary alcohols and both electron-rich and electron-poor alkenes, and gave the final products in moderate to high yields and excellent regioselectivities. Two α-substituted styrenes have also been tested and afforded the expected products in good yields. Notably, β-substituted styrenes were also tolerated under the reaction conditions, however, the diastereoselectivity of products was modest at best. The proposed mechanism for this transformation is shown in Scheme 8 which is based on a radical process. First, molecular iodine (I2) and methanethiol (MeSH) are formed from NH4I and DMSO through a series of reactions. Next, I2 is decomposed under the thermal condition to form iodine radical (I˙), which is later reacted with precursor MeSH resulting in a methylthiyl radical (MeSC˙) and concurrently abstracted a hydrogen atom from alcohols to afford alkoxy radical (ROC˙). Subsequently, addition of the methylthiyl radical to the CC double bond of alkene leads to an alkyl radical intermediate. Finally, the rapid combination of alkoxy radical and the newly formed carbon-centered radical delivers the desired product. Recently, Liu et al. extended the substrate scope of this reaction to aliphatic (terminal and internal) alkenes by performing the process in the presence of (COCl)2 in MeCN.25 Noteworthy, cycloalkenes selectively afforded trans-adducts under these conditions. Besides alcohols, carboxylic acids also could be applied as suitable O-nucleophiles under the identical conditions.
Scheme 7 Synthesis of β-alkoxy methyl sulfides 20 through the NH4I-mediated three-component coupling alkenes 17, dimethyl sulfoxide 18 and alcohols 19. |
In 2016, Lin and Guo realized the effectiveness of broadly available and bench-stable sulfonyl chlorides as sulfenylating agents in alkoxysulfenylation reactions of C–C double bonds.26 In this study, they showed that treatment of aromatic terminal alkenes 21 with arylsulfonyl chlorides 22 and aliphatic alcohols 23 in the presence of excess amounts of tetrabutylammonium iodide (TBAI) as a promoter and HBr as an acidic additive in toluene furnished the corresponding β-alkoxy sulfides 24 in good to excellent yields, ranging from 62% to 90% (Scheme 9a). Internal aliphatic alkenes were also found to be suitable substrates for this protocol as exemplified by the formation of (2-ethoxycyclohexyl) (p-tolyl)sulfane by using cyclohexene as the substrate. However, just like previous works, aromatic alcohols were inert in this transformation. The mechanism proposed by the authors to explain this difunctionalization reaction is analogous to the one depicted for in Scheme 2. Along this line, the same research group also reported that in the presence of over-stoichiometric amounts of NaI and HBr, styrene derivatives 25 were similarly coupled with various aryl/alkyl-sulfinic acids 26 and alkyl/benzyl-alcohols 27 to obtain β-alkoxy sulfide products 28 with yields of up to 95% (Scheme 9b).27
In 2018, Lei and co-workers developed an elegant electrochemical alkoxysulfenylation of alkenes 29 with thiols 30 and alcohols 31 under external oxidant-free conditions which exhibited better substrate scope compared to previously reported examples of this chemistry.28 The reactions were conducted in an undivided cell under a constant current of 12 mA cm−2 with carbon anode and platinum plate cathode employing nBu4NBF4 as the electrolyte and MeCN as the solvent at 40 °C, which afforded the β-alkoxy sulfide products 32 in 20–95% yields (Scheme 10). Noteworthy, other nucleophiles such as amines, acetic acid and water were also developed as the coupling partners in this reaction. Some important information of this oxidative sulfenylation reaction are listed below: (i) although both aromatic and aliphatic thiols were compatible with this reaction, aliphatic thiols afforded significantly poorer yields compared to aromatic ones; (ii) like previous works, the scope of alcohols was restricted to the use of aliphatic and benzylic alcohols; and (iii) the protocol for difunctionalization of aliphatic and internal alkenes was considerably less efficient than aromatic and terminal alkenes. According to the authors proposed mechanism (Scheme 11), this reaction proceeds through a thiiranium ion intermediate.
Scheme 11 A plausible mechanism for the reaction in Scheme 10. |
In 1987, Brownbridge introduced the use of N-(phenylthio)morpholine as an efficient phenylthiolating agent for intramolecular sulfenyl etherification of alkenols under metal-free conditions.33 Thus, a library of thiophenol-functionalized five-, six-, and seven-membered cyclic ethers 38 were successfully synthesized by treatment of the corresponding unsaturated alcohols 36 with N-(phenylthio)morpholine 37 in the presence of a stoichiometric amount of triflic acid (TfOH) as a promoter in a dry solvent at −20 °C (Scheme 13). However, cyclization to give four-membered ring systems did not take place by this method. Interestingly, when a cis-disubstituted alkenol (5-octen-1-ol) subjected to this reaction condition, a single regio- and stereo-isomer 38d was formed, indicated trans-addition without any alkene isomerization. Shortly afterwards, the author found that the regio- and stereo-selectivity of this cyclofunctionalization reaction is highly dependent on the substitution patterns of the employed alkenols.34 Benzenesulfenyl chloride was also found to be useful for the cyclization, though few examples are available.35–37
Drawing inspiration from these works, in 2011, Shi's group demonstrated an interesting acid-catalyzed regio- and stereo-selective sulfetherification of alkenols 39 with the use of N-(benzylthio)succinimide 40, thus providing either the corresponding tetrahydrofurans 41 and tetrahydropyrans 42 depending upon the acid catalyst used (Scheme 14).38 Studies indicated the formation of 5-exo cyclization products with camphorsulfonic acid (CSA) or tosylic acid (TsOH) and 6-endo cyclization products in the presence of triflic acid (TfOH). The results proved that cis-alkenes gave higher 5-exo selectivity as compared to trans-alkenes. The authors ascribed this observation by the steric effect during the cyclization. Studies also showed that when isolated 5-exo products were treated with a catalytic amount of TfOH at room temperature, 6-endo products were formed in high yields. These results clearly indicated that the cyclization route to tetrahydrofurans 41 was under kinetic control, while the formation of tetrahydropyrans 42 was thermodynamically favored.
Scheme 14 Acid-dependent regioselective sulfetherification of alkenols 39 in the presence of N-(benzylthio)succinimide 40 reported by Shi. |
Concurrently, Denmark and colleagues developed a robust asymmetric sulfetherification of various alkenols using a chiral BINAM-based selenophosphoramide catalyst 43 and a Brønsted acid (methanesulfonic acid, MsOH) additive.39 A library of conjugated and trans nonconjugated alkenes 44 reacted efficiently with N-phenylsulfenyl-phthalimide 45 in the presence of 10 mol% of 43 to afford sulfenylated tetrahydropyrans 46 in modest to excellent yields and outstanding enantioselectivities along with a small amount of sulfenylated tetrahydrofuran side-products (Scheme 15). Notably, when unsubstituted, cis nonconjugated and geminally disubstituted alkenes were subjected to the same reaction conditions, sulfenylated tetrahydrofurans were formed as the main reaction products, thus suggesting that the regioselectivity of this transformation is strongly dependent on the substitution patterns of the employed alkenols. Besides alkenols, unsaturated carboxylic acids could also be elegantly used in this cyclofunctionalization reaction. Moreover, several successful examples of the intermolecular sulfetherification of simple alkenes with methanol also reported under this reaction condition.
In a related investigation, Shi and co-workers reacted 5-substituted-pent-4-en-1-ols 47 with trifluoroethyl benzenesulfenate 48 in the presence of chiral tartaric acid-based catalyst 49 to selectively provide enantioenriched tetrahydrofurans 50 in good to excellent yields (68–90%) and low to good enantioselectivities (31–63% ee) (Scheme 16a).40 Although the reaction showed good tolerance to a series of cis-alkenols, trans-alkenols completely failed to participate in this transformation. Subsequently, Wu and Jiang along with their co-workers demonstrated the synthesis of a diverse range of sulfenylated four-, five-, six-, and seven-membered cyclic ether derivatives 53 via CuBr2-catalyzed sulfetherification of the corresponding alkenols 51 employing sodium sulfinates 52 as sulfenylating agents.41 The reaction was run in DMF at 120 °C, tolerated various aliphatic, benzylic, and (hetero)aromatic sodium sulfinates, and provided the desired sulfenylated O-heterocycles in good to excellent yield. However, the only example of strained four-membered ring product was obtained in medium yield. Some reported examples are shown in Scheme 16b. It should be mentioned that other simple copper salts such as CuCl, CuBr, CuI, and CuCl2 were also found to catalyze this sulfenylative cyclization reaction, albeit with reduced efficiencies. On the basis of a series of preliminary control experiments, it was suggested that this sulfetherification reaction starts with the formation of disulfide intermediate A via Cu-catalyzed dimerization of sodium sulfinate 52, which then undergoes radical cracking to give the sulfur radical B. Subsequently, this radical adds to the double bond of alkene 51 to form the α-sulfenyl-alkyl radical C that, after a single-electron oxidation converts to the carbocation D. Finally, the internal nucleophilic trapping of the newly formed intermediate D affords the desired product 53 (Scheme 17).
Scheme 17 Mechanism of the Cu(II)-catalyzed sulfetherification of alkenols 51 with sodium sulfinates 52. |
In 2017, Zhang, Yan, and Lin studied the possibility of synthesizing sulfenylated 2,3-dihydrobenzofurans through the intramolecular sulfetherification of 2-allylphenol 54 with environmentally friendly thiosulfates 55.42 To determine the best conditions, they meticulously probed the activities of different iodine-based catalysts (e.g., I2, NaI, TBAI, NH4I) and oxidants (e.g., H2O2, DMSO, TBHP, Cu(OAc)2, K2S2O8) in the sulfenyl etherification of 2-allylphenol with sodium S-benzyl sulfothioate in MeCN, as a model reaction. The optimal system was recognized with the used of 20 mol% NaI and 2 equiv. of DMSO at 100 °C. Under the optimized conditions, 2-allylphenol 54 was reacted with various aromatic, aliphatic, and benzylic thiosulfates 55 to provide the corresponding 2-(thiomethyl)-2,3-dihydrobenzofurans 56 in good to excellent yields within 3 h (Scheme 18). The authors have also examined pent-4-en-1-ol in place of 2-allylphenol to give the respective tetrahydrofuran in good yield. Furthermore, three component reaction between alkenes, acetic acid, and thiosulfates also successfully implemented under the identical conditions to provide the desired β-acetoxy sulfides in good yields.
Along this line, recently, Gao et al. found that a combination of dimethyl sulfoxide (DMSO) and oxalyl chloride [(COCl)2] is a suitable reagent for sulfenyletherification of unsaturated alcohols under catalyst- and additive-free conditions.43 Methanesulfenyl chloride (MeSCl) is assumed to be the compound responsible for the sulfenyletherification, which is generated by the reaction of DMSO and (COCl)2. Various unsaturated alcohols including 3, 4, and 5-alkenols were all compatible by this reaction, thus indicating its broad applicability. However, cis-3-alkenols 57 cannot be converted to cyclic ethers due to the effect of steric bulk in the intermediates. In these cases, instead of cyclic ethers, seven-membered cyclic acetals 58 with cis configurations were generated as the sole reaction products (Scheme 19a). According to the authors proposed mechanism (Scheme 19b), this transformation began with the addition of methanechloride to the double bond of cis-3-alkenol 57 to achieve cis-thiiranium ion intermediate A. Then, the oxygen of carbonyl group of formaldehyde, generated in situ during the formation of methanesulfenyl chloride, was attached at the less substituted carbon atom of thiiranium ion to form carbocation intermediate B. Finally, intramolecular cyclization of intermediate B led to the observed seven-membered cyclic acetal 58.
Scheme 19 (a) Gao's synthesis of seven-membered cyclic acetals 58; (b) plausible reaction mechanism for the formation of seven-membered cyclic acetals 58. |
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