Synthesis, Table of Contents PAPER© Georg Thieme Verlag Stuttgart · New YorkDirect Acylation of Phenol and Naphthol Derivatives in a Mixture of Graphite and Methanesulfonic Acid Hashem Sharghi*, Mona Hosseini-Sarvari*, Razieh EskandariDepartment of Chemistry, Faculty of Science, Shiraz University, Shiraz 71454, Irane-Mail: shashem@susc.ac.ir; e-Mail: hossaini@susc.ac.ir; Recommend Article Abstract Buy Article(opens in new window) All articles of this category(opens in new window) Abstract Graphite in methanesulfonic acid is used to prepare o-hydroxyketones by direct acylation of phenol and naphthol derivatives with carboxylic acids. Keyword graphite - methanesulfonic acid - o-hydroxyarylketones - direct acylation Full Text References References <A NAME="RZ22105SS-1">1</A> Healy PC. Mockler DP. Sinn E. J. Chem. Soc. 1975, 12: 691 <A NAME="RZ22105SS-2">2</A> Maeda Y. Noda Y. Oshio H. Takashima Y. Bull. Chem. Soc. Jpn. 1992, 65: 1825 <A NAME="RZ22105SS-3">3</A> McDonald PD. Hamilton GA. J. Am. Chem. Soc. 1973, 95: 7752 <A NAME="RZ22105SS-4">4</A> Van de Sanda C. Vondewalle M. Bull. Soc. Chim. Belg. 1973, 82: 705 <A NAME="RZ22105SS-5">5</A> Banerji A. Goomer NC. Synthesis 1980, 874 <A NAME="RZ22105SS-6">6</A> Lang G, Malaval A, and Leduc M. inventors; BE Patent 893250. ; Chem. Abstr. 1983, 98, 95499e <A NAME="RZ22105SS-7">7</A> Takanishi Y. Ouchi Y. Takezoe H. Fukuda A. Mochizuki A. Nakatsuka M. Mol. Cryst. Liq. Cryst. 1991, 199: 111 ; Chem. Abstr. 1991, 115, 102691m <A NAME="RZ22105SS-8">8</A> Martine R. Org. Prep. Proced. Int. 1992, 24: 369 <A NAME="RZ22105SS-9">9</A> Fodor G. Kiss J. Szekerke M. J. Org. Chem. 1950, 15: 227 <A NAME="RZ22105SS-10A">10a</A> Roberts RMG. Sadri AR. Tetrahedron Lett. 1983, 39: 137 <A NAME="RZ22105SS-10B">10b</A> Arata HM. J. Chem. Soc., Chem. Commun. 1986, 51: 2128 <A NAME="RZ22105SS-10C">10c</A> Chich B. Finiels A. Gauthier C. Geneste P. J. Org. Chem. 1986, 51: 2128 <A NAME="RZ22105SS-10D">10d</A> Keumi T. Yoshimura K. Shimada M. Kitajima H. Bull. Chem. Soc. Jpn. 1988, 61: 455 <A NAME="RZ22105SS-11">11</A> Kobayashi S. Moriwaki M. Hachiya I. Tetrahedron Lett. 1996, 12: 2053 <A NAME="RZ22105SS-12A">12a</A> Kagan HB. Pure Appl. Chem. 1976, 46: 177 <A NAME="RZ22105SS-12B">12b</A> Setton R. Intercalation Compounds of Graphite and their Reactions in Preparative Chemistry Using Supported Reagents Chap. 15: Lazlo P. Academic Press; London: 1987. p.255-283 <A NAME="RZ22105SS-12C">12c</A> Furstner A. Angew. Chem., Int. Ed. Engl. 1993, 32: 164 <A NAME="RZ22105SS-12D">12d</A> Wiesendanger R. Anlemetti D. Phys. Chem. Mater. Low-Dimens. Struct. 1992, 16: 1 <A NAME="RZ22105SS-12E">12e</A> Madsen LL. Joergensen JF. Camerio K. Synth. Met. 1993, 55: 335 <A NAME="RZ22105SS-13A">13a</A> Audhuy-Peaudecerf M, Berlan J, Dubac J, Laporterie A, Laurent R, and Lefeuvre S. inventors; French Patent 94/09073. <A NAME="RZ22105SS-13B">13b</A> Laurent R. Thesis Université Paul Sabatier; France: 1994. <A NAME="RZ22105SS-13C">13c</A> Laporte C. Thesis Université Paul Sabatier; France: 1997. <A NAME="RZ22105SS-13D">13d</A> Garrigues B. Laporte C. Laurent R. Laporterie A. Dubac J. Liebigs Ann. 1996, 739 <A NAME="RZ22105SS-13E">13e</A> Garrigues B. Laporte C. Laurent R. Laporterie A. Dubac J. Liebigs Ann. 1996, 743 <A NAME="RZ22105SS-13F">13f</A> Garrigues P. Garrigues B. C. R. Acad. Sci., Ser. IIc 1998, 1: 545 <A NAME="RZ22105SS-13G">13g</A> Laporte C. Oussaid A. Garrigues B. C. R. Acad. Sci., Ser. IIc 2000, 3: 321 <A NAME="RZ22105SS-14">14</A> Dabirmanesh Q. Fernando SIS. Roberts RMG. J. Chem. Soc., Perkin Trans. 1 1995, 643 <A NAME="RZ22105SS-15">15</A> Villemin D. Hachemi M. Lalaoui M. Synth. Commun. 1996, 2461 <A NAME="RZ22105SS-16">16</A> Marquie J. Laporterrie A. Dubac J. Roques N. Synlett 2001, 493 <A NAME="RZ22105SS-17A">17a</A> Sharghi H. Hosseini-Sarvari M. Synthesis 2003, 243 <A NAME="RZ22105SS-17B">17b</A> Hosseini-Sarvari M. Sharghi H. Helv. Chim. Acta 2005, 8: 2282 <A NAME="RZ22105SS-18A">18a</A> Sharghi H. Hosseini-Sarvari M. Synlett 2001, 99 <A NAME="RZ22105SS-18B">18b</A> Sharghi H. Hosseini-Sarvari M. Synthesis 2002, 1057 <A NAME="RZ22105SS-18C">18c</A> Sharghi H. Hosseini-Sarvari M. Tetrahedron 2002, 58: 10323 <A NAME="RZ22105SS-18D">18d</A> Sharghi H. Hosseini-Sarvari M. J. Chem. Res. 2001, 446 <A NAME="RZ22105SS-18E">18e</A> Sharghi H. Kaboudin B. J. Chem. Res., Synop. 1998, 628 <A NAME="RZ22105SS-19">19</A> Sharghi H. Hosseini-Sarvari M. Synthesis 2004, 2165 <A NAME="RZ22105SS-20">20</A> Ueda M. Sato M. Mochizuki A. Macromolecules 1985, 18: 2723 <A NAME="RZ22105SS-21">21</A> Handbook of Tables for Organic Compound Identification CRC Press; Boca Raton: 1973-1974. 54th edition and 1999-2000, 80th edition <A NAME="RZ22105SS-22">22</A> Matlloubi Moghaddam F. Ghaffarzadeh M. Abdi-oskoui SH. J. Chem. Res., Synop. 1999, 574 <A NAME="RZ22105SS-23">23</A> Salunkh MM. Nara SJ. Harjani JR. Tetrahedron Lett. 2001, 42: 1979