Characterizing Novel Methoxybenzene via Boron-ate Complex

Characterizing Novel Methoxybenzene via Boron-ate ComplexSynthesis and Characterization of Novel (E)-1-(hexa-3,5-dien-1-yl)-4-methoxybenzene via Boron-ate ComplexHabib Hussain*, Syeda Rubina Gilani, Zulfiqar Ali, Imdad Hussain, Hajira Rehman creepNovel (E)-1-(hexa-3,5-dien-1-yl)-4-methoxybenzene was synthesized through boron-ate complex. 3-(4-methoxyphenyl)propyl diisopropylcarbamate was reacted with allylboronic acid pinacol ester in the presence of N,N,N,N-tetramethylethyllenediamine (TMEDA) to confuse secondary boronic ester which was further reacted with (vinylsulfonyl)benzene by apply Grubbs Hoveyda II. Resulting product (E)-2-(1-(4-methoxyphenyl)-6-(phenylsulfonyl)hex-5-en-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane was then treated with 1-bromo-3,5-bis(trifluoromethyl)benzene in the presence of n-BuLi to get nucleophilic boron-ate complex. (E)-1-(hexa-3,5-dien-1-yl)-4-methoxybenzene was obtained in excellent yields by stirring boron-ate complex at 50oC for 1h and refluxing for 15h.Keywords Lithiation Borylation, Secondary Boronic Ester, olefin Cross Metathesis, 1-bromo-3,5-bis(trifluoromethyl)benzene , Boron-ate Complex1. IntroductionOlefin metathesis chemistry1 has led a number of opportunities in perfect synthesis. Olefin metathesis2involves the redistribution of fragments ofalkenes by regeneration of carbon-carbondouble bonds. There are numerous applications of olefin metathesis and it is an main(prenominal) methodology to produce reagents.Addition of aryl lithium reagents to secondary boronic esters results to a new class of chiral organometallic-type reagents which have broad utility in asymmetric organic synthesis. R. Larouche-Gauthier3 formed intermediate boron-ate complex by adding an aryllithium reagent to a secondary boronic ester. It behaved as a chiral nucleophile and maximum enantioselectivity was found by using electron withdrawing groups on aryllithium. Habib Hussain4 studied the effect of steric bulk of aryllithium on stereoselectiv ity of boron-ate complexes. Hoffmann5 obtained chiral Grignard reagents from sulfoxides Mg exchange reaction of halosulfoxides. Herbert C. Brown6 investigated iodination of the ate- complexes from various B-alkoxyborinane derivatives and 1-alkynyllithium. E. Vedejs7 synthesized ate- complexes which contained stereogenic boron by reacting trivalent boranes with nucleophiles. They noticed that stability of ate-complex depend upon the negativeness of substituents attached to boron. Ryschkewitsch, G. E8 resolved chiral boron-ate complexes by classical methods. Anna Bernardi 9 determined the role of ate-complxes im aldol stereoselectivity.In the recent paper, we reported the synthesis of Novel (E)-1-(hexa-3,5-dien-1-yl)-4-methoxybenzene (7). It was lineamentized by IR, 1H, 13C and ms. Lithiation-Borylation was use to synthesize the secondary boronic ester and by using olefin cross metathesis, it gave (E)-2-(1-(4-methoxyphenyl)-6-(phenylsulfonyl)hex-5-en-3-yl)-4,4,5,5-tetramethyl-1,3,2- dioxaborolane when reacted with (vinylsulfonyl)benzene. (E)-2-(1-(4-methoxyphenyl)-6-(phenylsulfonyl)hex-5-en-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane was converted into ate-complex when on heating produced the desired product.2. Experimental Section2.1. Materialsn-butyllithium (nBuLi), sec. butyllithium solution (sBuLi) (1.6M), pinacol, N,N,N,N-tetramethylethyllenediamine (TMEDA), (vinylsulfonyl)benzene, Grubbs Hoveyda II and 1-bromo-3,5-bis(trifluoromethyl)benzene were purchased from Sigma Aldrich. All reagents were used as such as received. To avoid from moisture diethyl ether (Et2O) and tetrahydrofuran (THF) were dried with 4 A molecular sieves. The experiments were performed using schlenk line downstairs nitrogen atmosphere in the absence of air and moisture.2.2. Synthesis and Characterization of 2-(1-(4-methoxyphenyl)hex-5-en-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (3)To a solution of 3-(4-methoxyphenyl)propyl diisopropylcarbamate (1.0g, 3.41mmol, 1.0eq) (1) and N, N,N,N-tetramethylethyllenediamine (TMEDA) (0.61mL, 4.09mmol, 1.2eq) (2a) in Et2O (17mL) at -78oC, Sec. BuLi (1.6M in 928 cyclohexane/hexane, 2.9mL, 3.75mmol, 1.1eq) was dropwise added and aroused for 5h at -78oC. Then allylboronic acid pinacol ester (0.77mL, 4.09mmol, 1.2eq) (2) was dropwise added to the reaction mixture and further stirred at -78oC for 1h and allowed to warm to room temperature. At this stage, a solution of MgBr2.OEt2 in Et2O, do as follows, was added to the reaction mixture. At room temperature, 1,2-dibromoethane (0.60mL, 6.88mmol, 1.0eq) was added into a suspension of magnesium (0.17g, 6.88mmol, 1.0eq) in Et2O (8.6mL). The reaction flask was further stirred for 2h after placing into a water tub in order to control the moderate exotherm. Biphasic mixture having two layers thus obtained was added to the former reaction mixture via syringe and then refluxed for 16h. after(prenominal) cooling the reaction mixture to room temperature it was quenched with water. Et2O was added, the layers were separated and the aqueous phase was extracted with Et2O. The combined organic layers were washed with 1N HCl, 1N NaOH, water and brine, dried (MgSO4), concentrated and purified by editorial chromatography (SiO2) and smooth (R)-2-(1-(4-methoxyphenyl)hex-5-en-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (3) (0.84g, 77.60%) was obtained as colorless oil. The reaction is given in Figure 1.1H nuclear magnetic resonance (400 MHz, CDCl3) ppm 7.09 (2H, d, J=8.80 Hz, 2 ArH) 6.81 (2H, d, J=8.80 Hz, 2 ArH) 5.86 5.75 (1H, m, CH=CH2) 5.04 (1H, d, J=2.20 Hz, CH=CHH) 4.94 (1H, d, J=10.27 Hz, CH=CHH) 3.78 (3H, s, OCH3) 2.63 2.48 (2H, m, ArCH2CH2CHBCH2) 2.27 2.11 (2H, m, ArCH2CH2CHBCH2) 1.78 1.58 (2H, m, ArCH2CH2CHBCH2) 1.25 (12H, s, 4 CH3) 1.08 1.18 (1H, m, ArCH2CH2CHBCH2)13C proton magnetic resonance (100 MHz, CDCl3) ppm 157.6 (1C, -OCH3), 138.4 (2C, 2 ArCH), 135.0 (2C, 2 ArCH), 129.2 (1C, ArC-O), 114.9 (1C, -CH2CH=CH2), 113.6 (1C, -CHb=CH2), 83.0 (2C, 2 C(CH3)2), 55.2 (1C, ArCCH2), 35.3 (1C, CH2CH2CHB), 34.5 (1C, -CH2CHB), 33.1 (1C, -CHBCH2CH), 24.9 (1C, -CH2CH2CHB), 24.8 (4C, 2 (CH3)2C).11B NMR (96.23 MHz, None) ppm 33.24IR (film) (cm1) 3026 (sp2C-H Stretch), 2977, 2924, 2852 (sp3 C-H Stretch), 1511, 1456(sp2 C=C Stretch), 1243, 1175, 1142 (sp3C-O Stretch), 846, 822, 670 (sp2 C-H oop bending).2.3. Synthesis and Characterization of (E)-2-(1-(4-methoxyphenyl)-6-(phenylsulfonyl)hex-5-en-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (5)Grubbs-Hoveyda II (4a) (3.9mg, 0.0063mmol, 0.05eq) was added to a solution of 2-(1-(4-methoxyphenyl)hex-5-en-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (3) (40mg, 0.126 mmol, 1.0eq) and (vinylsulfonyl)benzene (4) (0.0635g, 0.378mmol, 3.0eq) in CH2Cl2 (2mL). After fitting a condenser to the flask, reaction mixture was refluxed for 15h under nitrogen. The reaction mixture was then reduced in volume to 0.5mL and purified directly on a silica gel column eluting with 91 Pet. Ether/ EtOAc to provide th e desired product (E)-2-(1-(4-methoxyphenyl)-6-(phenylsulfonyl)hex-5-en-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (5) as dark brown solid (0.0438g, 77.25%)10.m.p. 82.0oC1H NMR (400 MHz, CDCl3) ppm 7.88-7.84 (2H, m, 2 ArH) 7.62-7.56 (1H, m, , 1 ArH) 7.54-7.48 (2H, m, 2 ArH) 7.05-6.99 (2H, m, 2 ArH) 6.96 (1H, t, J=6.97 Hz, CH2-CH=CH) 6.84-6.77 (2H, m, 2 ArH) 6.31 (1H, dt, J=15.16, 1.47 Hz, CH2-CH=CH) 3.78 (3H, s, -CH3) 2.59-2.45 (2H, m, CH2-CH2-CHB) 2.43-2.26 (2H, m, CH2-CHB-CH2) 1.77-1.66 (1H, m, CH2-CHB-CHH) 1.63-1.53 (1H, m, CH2-CHB-CHH) 1.27-1.21 (1H, m, CH2-CHB-CH2) 1.18 (12 H, s, 4 CH3)13C NMR (100 MHz, CDCl3) ppm 157.7 (1C, ArC-O) 146.9 (1C, ArC-S) 140.8 (1C, CH=CH-S) 134.2 (1C, CH=CH-S) 133.1 (1C, ArC-CH2) 130.6 (1C, ArCH) 129.2 (2C, 2 ArCH) 129.1 (2C, 2 ArCH) 127.5 (2C, 2 ArCH) 113.7 (2C, 2 ArCH) 83.4 (2C, 2 C(CH3)2) 55.2 (1C, OCH3) 34.1 (1C, CH2CHBCH2) 33.1 (1C, CH2CH2CHB) 32.8 (4C, 2 (CH3)2C) 24.8 (1C, -CHBCH2CH) 24.7 (1C, CH2CH2CHB)11B NMR (96.23 MHz, Non e) ppm 33.24IR (film) (cm1) 2977, 2924 (sp3 C-H Stretch), 1511, 1446(sp2 C=C Stretch), 1244, 1176, 1141 (sp3C-O Stretch), 822, 730, 687 (sp2 C-H oop bending).2.4. Synthesis and Characterization of (E)-1-(hexa-3,5-dien-1-yl)-4-methoxybenzene (7)To a solution of 3,5-(CF3)2C6H3Br (24.6mg, 0.084mmol, 1.2eq) in THF (1.9mL) at -78oC was added n-BuLi (1.6M in hexanes, 0.053mL, 0.084mmol, 1.2eq) dropwise. The mixture was stirred for 1 hr at -78oC before a solution of boronic ester (32mg, 0.070mmol, 1.0eq) in THF (1.5mL) was added dropwise. The reaction mixture was stirred for 30min at -78oC and 30min at room temperature to form boron-ate complex which was further heated up at 50oC for 1 hr and refluxed for 15hr.Reaction was quenched with water, EtOAc was added and layers were separated. The aqueous phase was extracted with EtOAc. Then layers were combined, washed with brine, dried (MgSO4), concentrated. The crude mixture was finally purified by column chromatography (SiO2, 21 Pet.Ether/Et OAc) to get desired product as colorless oil (19.87mg, 62.10%).1H NMR (400 MHz, CDCl3) ppm 7.14-7.07 (2H, m, 2 ArH) 6.85 6.80 (2H, m, 2 ArH) 6.30 (1H, dt, J=17.00, 10.21 Hz, CH=CH-CH=CH2) 6.12-5.97 (1H, m, CH=CH-CH=CH2) 5.78-5.69 (1H, m, CH=CH-CH=CH2) 5.21-5.06 (1H, m, CH=CHH) 4.99-4.95 (1H, m, CH=CHH) 3.79 (3H, s, -CH3) 2.70-2.60 (2H, m, CH2CH2CH) 2.52-2.33 (2H, m, CH2CH2CH)13C NMR (100 MHz, CDCl3) ppm 157.7 (1C, ArC-O) 137.0 (1C, CH=CH2) 133.7 (1C, CH=CH-CH=CH2) 132.0 (1C, ArC-CH2) 129.5 (1C, CH=CH-CH=CH2) 129.1 (2C, 2 ArCH) 114.9 (1C, CH=CH2) 113.6 (2C, 2 ArCH) 55.1 (1C, CH3) 34.6 (1C, CH2CH2CH) 34.5 (1C, CH2CH2CH)IR (film) (cm1) 2955, 2921, 2852 (sp3 C-H Stretch), 1737, 1461(sp2 C=C Stretch), 1277, 1184, 1137 (sp3C-O Stretch), 967, 805 (sp2 C-H oop bending).HRMS (ESI) calcd. for C13H17O M+H+ 189.1279, found 189.1287.2.5. Equipments1H and 13C spectral measurements were done by using Varian NMR (400 MHz) spectrometer (model DMX 400). For protons, the chemical shifts were m easured relative to tetramethylsilane (TMS) at d = 0 ppm.3. Results and DiscussionStarting material 2-(1-(4-methoxyphenyl)hex-5-en-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (3) has been synthesized as colorless oil in excellent yields (77.6%) (table 1, entry 1) by using Lithiation-Borylation methodology Carbamate (1) was reacted with pinacol (2) by using TMEDA (2a) at suitable conditions (fig.1). Spectral studies proved the structure as mentioned in literature11. By using application of olefin cross metathesis, boronic ester (3) was then reacted with (vinylsulfonyl)benzene (4) to give (E)-2-(1-(4-methoxyphenyl)-6-(phenylsulfonyl)hex-5-en-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (5) as dark brown solid. Yield was again excellent (table 1, entry 2) for this reaction.Table 1 Physical states and yieldsEntrySubstancesPhysical StatesMelting pointsYield (%)1Colorless oil77.602Dark brown solid82.0oC77.253Colorless oil62.10Boron-ate complex (6) which acted as nucleophile was synthes ized by reacting (E)-2-(1-(4-methoxyphenyl)-6-(phenylsulfonyl)hex-5-en-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (5) with aryllithium (5a). Boron-ate complex (6) showed best nucleophilic character by using 3,5-(CF3)2C6H3Br (5a) as aryllithium11 and it was then stirred at 50oC for 1hr and then refluxed for 15hrs and desired product (E)-1-(hexa-3,5-dien-1-yl)-4-methoxybenzene (7) was collected.4. ConclusionsNovel (E)-1-(hexa-3,5-dien-1-yl)-4-methoxybenzene has been synthesized through a novel route and characterized by spectral techniques like IR, 1H, 13C and ms. Boron-ate complex was successfully converted into aromatic dienes. This novel synthetic route resulted in excellent yields.AcknowledgmentAuthors gratefully acknowledge fiscal support to the work by Higher Education Commission of Pakistan and moreover authors acknowledge the Department of Chemistry, University of Engineering and Technology, Lahore-Pakistan and Superior University Lahore-Pakistan for guidance, research and laboratory facilities.ReferencesGrubbs, R. H. Chang, S. Tetrahedron 1998, 54, 44134450Astruc D. New J. Chem., 2005, 29, 42-56.R. Larouche-Gauthier, T.G. Elford and V.K. Aggarwal, J. Am. Chem.Soc., 2011,133, 16794.Habib Hussain, Syeda Rubina Gilani, Zulfiqar Ali and Imdad Hussain, Asiatic Journal of Chemistry 2013, 25, 17, 9965-9969Hoffmann, R. W. Chem. Soc. Rev. 2003, 32, 225.Herbert C. Brown, D. Basavaiah, and N. G. Bhat, D. Basavaiah, and N. G. Bhat, J. Org. Chem. 1986, 51, 4518-4521E. Vedejs, S. C. Fields, S. Lin, and M. R. Schrimpf, J. Org. Chem. 1995, 60, 3028-3034.Ryschkewitsch, G. E. Garrett, J. M. J. Am. Chem. Soc. 1968, 90, 7234.Anna Bernardi, Angiolina Comotti, Cesare Gennari, Cheryl T. Hewkin, Jonathan M. Goodman, Achim Schlapbach and Ian Paterson, Tetrahedron 50, 4, 1227-1242, 1994.Bruce H. Lipshutz, Subir Ghorai, Zarko V. Boskovic, Tetrahedron, 64, 29, 2008, 6949-6954.Habib Hussain, Syeda Rubina Gilani, Zulfiqar Ali and Imdad Hussain, Asian Journal of Chemistry, In Pre ss.*Corresponding Author Habib Hussain