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Novel alkali-promoted hydrotalcite for selective synthesis of 2-methoxy phenyl benzoate from guaiacol and benzoic anhydride

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Abstract

Esters find several applications such as solvents, flavours and fragrants and intermediates in synthesis of drugs. In the present work, 2-methoxy phenyl benzoate was efficiently synthesized from guaiacol and benzoic anhydride by acylation. A variety of catalysts such as hydrotalcite and alkali-promoted hydrotalcite was synthesized. Potassium-promoted hydrotalcite (K/HT) calcined at 500 °C for 6 h was active, selective and reusable. It was characterized by different techniques. A slurry batch reactor was used to study reaction mechanism and kinetics. 2-Methoxy phenyl benzoate was efficiently obtained with 100% selectivity at guaiacol conversion of 98% over K/HT at 100 °C after 6 h. A power law model with second-order kinetics was fitted to obtain an apparent activation energy of reaction of 21.1 kcal mol−1. The process is clean and green.

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Abbreviations

A :

Reactant species A, guaiacol

B :

Reactant species B, benzoic anhydride

D :

Product species D, 2-methoxy phenyl benzoate

E :

Product species E, benzoic acid

AS 1 :

Chemisorbed guaiacol on vacant sites of type S 1

BS 2 :

Chemisorbed benzoic anhydride on vacant sites of type S 2

DS 2 :

Chemisorbed 2-methoxy phenyl benzoate on vacant sites of type S 2

ES 1 :

Chemisorbed benzoic acid on vacant sites of type S 1

C A :

Concentration of A, guaiacol (mol L−1)

\(C_{{A_{0} }}\) :

Initial concentration of A in bulk liquid phase (mol L−1)

\(C_{{AS_{1} }}\) :

Adsorption concentration of A on active site S 1 (mol g−1 of cat)

C B :

Concentration of B, benzoic anhydride (mol L−1)

\(C_{{B_{0} }}\) :

Initial concentration of B in bulk liquid phase (mol L−1)

\(C_{{BS_{2} }}\) :

Adsorption concentration of B on active site S 2 (mol g−1 of cat)

C D :

Concentration of D, 2-methoxy phenyl benzoate (mol L−1)

\(C_{{DS_{2} }}\) :

Concentration of D on active sites of type S 2 (mol g−1 of cat)

C E :

Concentration of E, benzoic acid (mol L−1)

\(C_{{ES_{1} }}\) :

Concentration of E on active sites of type S 1 (mol g−1 of cat)

\(C_{{S_{1} }}\) :

Concentration of vacant sites of type S 1 (mol g−1 of cat)

\(C_{{S_{2} }}\) :

Concentration of vacant sites of type S 2 (mol g−1of cat)

\(C_{{{\text{T}}_{1} }}\) :

Total concentration of vacant sites of type S 1 (mol g−1 of cat)

\(C_{{{\text{T}}_{2} }}\) :

Total concentration of vacant sites of type S 2 (mol g−1 of cat)

C T :

Total concentration of sites (mol g−1 of cat)

K A :

Adsorption constant for A (L mol−1)

K B :

Adsorption constant for B (L mol−1)

K D :

Adsorption constant for D (L mol−1)

K E :

Adsorption constant for E (L mol−1)

1/K D :

Desorption constant for D from catalyst site S 2 (L mol−1)

1/K E :

Desorption constant for E from catalyst site S 1 (L mol−1)

k 1 :

Forward reaction rate constant for surface reaction (L2 mol−1 s−1 g-cat−1)

\(k_{1}^{\prime }\) :

Backward reaction rate constant for surface reaction (L2 mol−1 s−1 g-cat−1)

k 2 :

Second-order rate constant (L mol−1 s−1)

M :

Molar ratio of \({{C_{{B_{0} }} } \mathord{\left/ {\vphantom {{C_{{B_{0} }} } {C_{{A_{0} }} }}} \right. \kern-0pt} {C_{{A_{0} }} }}\)

r A :

Rate of reaction (mol L−1 min−1)

w :

Catalyst loading (g L−1)

X A :

Fractional conversion of A

t :

Time (min)

References

  • Balaskar RS, Gavade SN, Mane MS, Shingare MS, Mane DV (2011) Morpholinium bisulfate [morH][HSO4]-promoted O, S, and N acylation at room temperature. Green Chem Lett Rev 4:91–95. doi:10.1080/17518253.2010.504751

    Article  CAS  Google Scholar 

  • Ballini R, Bosica G, Carloni S, Ciaralli L, Maggi R, Sartori G (1998) Zeolite HSZ-360 as a new reusable catalyst for the direct acetylation of alcohols and phenols under solventless conditions. Tetrahedron Lett 39:6049–6052. doi:10.1016/S0040-4039(98)01244-1

    Article  CAS  Google Scholar 

  • Bartoli G, Bosco M, Dalpozzo R, Marcantoni E, Massaccesi M, Rinaldi S, Sambri L (2003) Mg(ClO4)2 as a powerful catalyst for the acylation of alcohols under solvent-free conditions. Synlett 2003:0039–0042. doi:10.1055/s-2003-36228

    Google Scholar 

  • Chakraborti AK, Gulhane R (2003) Indium(III) chloride as a new, highly efficient, and versatile catalyst for acylation of phenols, thiols, alcohols, and amines. Tetrahedron Lett 44:6749–6753. doi:10.1016/S0040-4039(03)01641-1

    Article  CAS  Google Scholar 

  • Dalpozzo R, De Nino A, Maiuolo L, Procopio A, Nardi M, Bartoli G, Romeo R (2003) Highly efficient and versatile acetylation of alcohols catalyzed by cerium (III) triflate. Tetrahedron Lett 44:5621–5624. doi:10.1016/S0040-4039(03)01358-3

    Article  CAS  Google Scholar 

  • Gore PH (1955) The Friedel–Crafts acylation reaction and its application to polycyclic aromatic hydrocarbons. Chem Rev 55:229–281. doi:10.1021/cr50002a001

    Article  CAS  Google Scholar 

  • Jin TS, Ma YR, Zhang ZH, Li TS (1998) Sulfamic acid catalysed acetylation of alcohols and phenols with acetic anhydride. Synth Commun 28:3173–3177. doi:10.1080/00397919808004417

    Article  CAS  Google Scholar 

  • Lavoie JM, Baré W, Bilodeau M (2011) Depolymerization of steam-treated lignin for the production of green chemicals. Bioresour Technol 102:4917–4920. doi:10.1016/j.biortech.2011.01.010

    Article  CAS  Google Scholar 

  • Liu Z, Ma Q, Liu Y, Wang Q (2014) 4-(N, N-dimethylamino)pyridine hydrochloride as a recyclable catalyst for acylation of inert alcohols: substrate scope and reaction mechanism. Org Lett 16:236–239. doi:10.1021/ol4030875

    Article  CAS  Google Scholar 

  • Massah AR, Kalbasi RJ, Toghiani M, Hojati B, Adibnejad M (2012) Hydrotalcite as an efficient and reusable catalyst for acylation of phenols, amines and thiols under solvent-free conditions. Eur J Chem 9:2501–2508. doi:10.1155/2012/872509

    CAS  Google Scholar 

  • Mirk D, Willner A, Fröhlich R, Waldvogel SR (2004) Iodinated biaryls synthesized by the direct dehydrodimerization of iodoarenes using phenyliodine(III) bis(trifluoroacetate) (PIFA). Adv Synth Catal 346:675–681. doi:10.1002/adsc.200404024

    Article  CAS  Google Scholar 

  • Naeimi H, Amini A, Moradian M (2014) Regioselective direct ortho C-acylation of phenol and naphthol derivatives catalyzed by modified ZnCl2 on Al2O3 as catalyst under solvent-free and microwave conditions. Org Chem Front 1:415–421. doi:10.1039/C4QO00031E

    Article  CAS  Google Scholar 

  • Phukan P (2004) Iodine as an extremely powerful catalyst for the acetylation of alcohols under solvent-free conditions. Tetrahedron Lett 45:4785–4787. doi:10.1016/j.tetlet.2004.04.076

    Article  CAS  Google Scholar 

  • Ralston AW, McCorkle MR, Bauer ST (1940) Orientation in the acylation of phenol and in the rearrangement of phenolic esters. J Org Chem 05:645–659. doi:10.1021/jo01212a011

    Article  CAS  Google Scholar 

  • Romanelli GP, Bennardi DO, Autino JC, Baronetti GT, Thomas HJ (2008) A simple and mild acylation of alcohols, phenols, amines, and thiols with a reusable heteropoly acid catalyst (H6P2W18O62·24 H2O). Eur J Chem 5:641–647. doi:10.1155/2008/945898

    CAS  Google Scholar 

  • Satam JR, Jayaram RV (2008) Acetylation of alcohols, phenols and amines using ammonium salt of 12-tungstophosphoric acid: environmentally benign method. Catal Commun 9:2365–2370. doi:10.1016/j.catcom.2008.05.033

    Article  CAS  Google Scholar 

  • Sheldon RA (2012) Fundamentals of green chemistry: efficiency in reaction design. Chem Soc Rev 41:1437–1451. doi:10.1039/C1CS15219J

    Article  CAS  Google Scholar 

  • Shivani, Gulhane R, Chakraborti AK (2007) Zinc perchlorate hexahydrate [Zn(ClO4)2·6H2O] as acylation catalyst for poor nucleophilic phenols, alcohols and amines: scope and limitations. J Mol Catal A Chem 264:208–213. doi:10.1016/j.molcata.2006.09.015

    Article  CAS  Google Scholar 

  • Yadav GD (2005) Synergism of clay and heteropoly acids as nano-catalysts for the development of green processes with potential industrial applications. Catal Surv Asia 9:117–137

    Article  CAS  Google Scholar 

  • Yadav GD, Aduri P (2012) Aldol condensation of benzaldehyde with heptanal to jasminaldehyde over novel Mg–Al mixed oxide on hexagonal mesoporous silica. J Mol Catal A Chem 355:142–154

    Article  CAS  Google Scholar 

  • Yadav GD, Bokade VV (1996) Novelties of heteropoly acid supported on clay: etherification of phenethyl alcohol with alkanols. Appl Catal A Gen 147:299–323

    Article  CAS  Google Scholar 

  • Yadav GD, Chandan PA (2014) A green process for glycerol valorization to glycerol carbonate using heterogeneous base catalyst. Catal Today 237:47–53

    Article  CAS  Google Scholar 

  • Yadav GD, Doshi NS (2002) Development of a green process for poly-α-olefin based lubricants. Green Chem 4:528–540

    Article  CAS  Google Scholar 

  • Yadav GD, Fernandes GP (2013) Selective synthesis of natural benzaldehyde by hydrolysis of cinnamaldehyde using novel hydrotalcite catalyst. Catal Today 207:162–169

    Article  CAS  Google Scholar 

  • Yadav GD, Joshi A (2002) A green route for the acylation of resorcinol with acetic acid. Clean Technol Environ Policy 4:157–164. doi:10.1007/s10098-002-0148-9

    Article  CAS  Google Scholar 

  • Yadav GD, Kadam AA (2013) Selective engineering using Mg–Al calcined hydrotalcite and microwave irradiation in mono-transesterification of diethyl malonate with cyclohexanol. Chem Eng J 230:547–557

    Article  CAS  Google Scholar 

  • Yadav GD, Kirthivasan N (1995) Single-pot synthesis of methyl tert-butyl ether from tert-butyl alcohol and methanol: dodecatungstophosphoric acid supported on clay as an efficient. JCS Chem Commun. doi:10.1039/C39950000203

  • Yadav GD, Nair JJ (2000) Isomerization of citronellal to isopulegol using eclectically engineered sulfated zirconia-carbon molecular sieve composite catalysts, UDCaT-2. Langmuir 16:4072–4079

    Article  CAS  Google Scholar 

  • Yadav GD, Rahuman MSMM (2002) Cation-exchange resin-catalysed acylations and esterifications in fine chemical and perfumery industries. Org Process Res Dev 6:706–713. doi:10.1021/op0255229

    Article  CAS  Google Scholar 

  • Yadav GD, Salunke JY (2013) Selectivity engineering of solid base catalysed O-methylation of 2-naphthol with dimethyl carbonate to 2-methoxynaphthalene. Catal Today 207:180–190

    Article  CAS  Google Scholar 

  • Yadav GD, Surve PS (2013) Solventless green synthesis of 4-O-aryloxy carbonates from aryl/alkyl-oxy propanediols and dimethyl carbonate over nano-crystalline alkali promoted alkaline earth metal oxides. Catal Sci Technol 3:2668–2676

    Article  CAS  Google Scholar 

  • Yadav GD, Goel PK, Joshi AV (2001) Alkylation of dihydroxybenzenes and anisole with methyl-tert-butyl ether (MTBE) over solid acid catalysts. Green Chem 3:92–99

    Article  CAS  Google Scholar 

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Acknowledgements

S.L.B. expresses thanks to the UGC for giving basic research (senior) fellowship. G.D.Y. acknowledges support from R. T. Mody Distinguished Professor Endowment of ICT and J. C. Bose National Fellowship of DST-GOI.

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Correspondence to Ganapati D. Yadav.

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Bhanawase, S.L., Yadav, G.D. Novel alkali-promoted hydrotalcite for selective synthesis of 2-methoxy phenyl benzoate from guaiacol and benzoic anhydride. Clean Techn Environ Policy 19, 1169–1180 (2017). https://doi.org/10.1007/s10098-016-1316-7

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