Rapid and clean synthesis of phthalimide derivatives in high-temperature, high-pressure H2O/EtOH mixtures

A variety of phthalimide derivatives have been synthesised effectively in high-temperature, high-pressure H2O/EtOH mixtures (HTHP-H2O/EtOH) as the solvent. This clean method is based on the condensation of o-phthalic acid and amines and affords phthalimide compounds as pure crystals in most cases, because of the dehydrating effect and change in solvation properties of H2O/EtOH at high pressures and temperatures. After conducting a series of model reactions, it was found that a mixture, 1/1 v/v H2O/EtOH, was appropriate for obtaining good yields combined with high purity of the phthalimides. Moderate to excellent yields were obtained depending on the nature of the amine. Aromatic amines generally afforded higher yields than aliphatic ones except for 3-hydroxypropylamine, where a yield up to 95% was obtained.

[1]  L. M. Lima,et al.  Synthesis and anti-inflammatory activity of phthalimide derivatives, designed as new thalidomide analogues. , 2002, Bioorganic & medicinal chemistry.

[2]  A. J. Blake,et al.  Synthesis of benzimidazoles in high-temperature water , 2003 .

[3]  M. Heravi,et al.  Synthesis of N-arylphthalimides catalyzed by 1,4-diazabicyclo[2,2,2]octane [DABCO] in solventless system , 2005 .

[4]  F. C. F. de Brito,et al.  Novel phthalimide derivatives, designed as leukotriene D(4) receptor antagonists. , 2002, Bioorganic & medicinal chemistry letters.

[5]  M. Poliakoff,et al.  Organic reactions in high-temperature and supercritical water , 2006 .

[6]  K. Weisgraber,et al.  Pigments of Elsinoe species. Part VI. A simple synthesis of a related perylenequinone , 1972 .

[7]  F. Barr-David,et al.  Vapor-Liquid Equilibrium at High Pressures. The Systems Ethanol-Water and 2-Propanol-Water. , 1959 .

[8]  E. W. Meijer,et al.  Synthesis of 3,6-diaminophthalimides for ureidophthalimide-based foldamers. , 2006, Organic letters.

[9]  Photocyclization of N-Alkoxyalkylphthalimides with Favored δ-Hydrogen Abstraction : Syntheses of Oxazolo [4, 3-α] isoindoles and Oxazolo [4, 3-α]-isoindole-1-spiro-1'-cycloalkane Ring Systems , 1982 .

[10]  J. Robert,et al.  New anti-inflammatory N-pyridinyl(alkyl)phthalimides acting as tumour necrosis factor-alpha production inhibitors. , 2001, European journal of medicinal chemistry.

[11]  J. Tingle,et al.  INTRAMOLECULAR REARRANGEMENT OF PHTHALAMIDIC ACIDS. III. , 1908 .

[12]  A. Abdel-Hafez Synthesis and anticonvulsant evaluation ofN-substituted-isoindolinedione derivatives , 2004, Archives of pharmacal research.

[13]  Bao-zeng Ren,et al.  Solubility of o-Phthalic Acid in Methanol + Water and Methanol + Butyl Acetate from (295.87 to 359.75) K , 2006 .

[14]  Victor Sans,et al.  Pd(0) supported onto monolithic polymers containing IL-like moieties. Continuous flow catalysis for the Heck reaction in near-critical EtOH. , 2006, Chemical communications.

[15]  Lallan P. Gupta,et al.  Thermal stability of amino acids in seafloor sediment in aqueous solution at high temperature , 2006 .

[16]  A. Grabowska,et al.  Single versus double proton transfer in the photochromic Schiff bases. Electronic spectroscopy and synthesis of model compounds , 1993 .

[17]  Z. Parveen,et al.  The cyclisation of substituted phthalanilic acids in acetic acid solution. A kinetic study of substituted N-phenylphthalimide formation , 2001 .

[18]  T. Matsuda,et al.  Reactions of supercritical alcohols with unsaturated hydrocarbons , 2003 .

[19]  A. Karim,et al.  Metal ions and complexes in organic reactions. Part XV. Copper-catalysed substitutions of aryl halides by phthalimide ion , 1973 .

[20]  M. Poliakoff,et al.  Simultaneous continuous partial oxidation of mixed xylenes in supercritical water , 2005 .

[21]  J. S. Sandhu,et al.  Microwave-induced One-pot Synthesis of N-carboxyalkyl Maleimides and Phthalimides† , 1998 .

[22]  K. Booksh,et al.  Monitoring anhydride and acid conversion in supercritical/hydrothermal water by in situ fiber-optic Raman spectroscopy , 1998 .

[23]  J. Baruah,et al.  Structural aspects of adducts of N-phthaloylglycine and its derivatives , 2006 .

[24]  J. Dávalos,et al.  The Elusive Antiaromaticity of Maleimides and Maleic Anhydride: Enthalpies of Formation of N-Methylmaleimide, N-Methylsuccinimide, N-Methylphthalimide, and N-Benzoyl-N-methylbenzamide. , 1997, The Journal of organic chemistry.

[25]  J. Verbicky,et al.  Thermolysis of N-alkyl-substituted phthalamic acids. Steric inhibition of imide formation , 1981 .

[26]  R. Srivastava,et al.  New phthalimide derivatives with potent analgesic activity: II. , 1998, Bioorganic & medicinal chemistry letters.

[27]  M. Sherrill,et al.  THE ISOMERISM OF PHENYLPHTHALIMIDE AND A STUDY OF THE NITRO AND CHLORO DERIVATIVES , 1928 .

[28]  A. Apelblat,et al.  The solubilities of benzene polycarboxylic acids in water , 2006 .

[29]  C. Chassaing,et al.  Microwave-assisted solid-phase synthesis of phthalimides. , 2003, Organic letters.

[30]  Jian Shen,et al.  Synthesis and characterization of water-soluble O-succinyl-chitosan , 2003 .

[31]  A. Petit,et al.  Re-examination of Microwave-Induced Synthesis of Phthalimides , 2000 .

[32]  J. Vernon,et al.  Some isoindolo-fused heterocyclic systems by cyclodehydration of N-arylalkyl-3-hydroxyphthalimidines , 1990 .

[33]  E. Muniz,et al.  Depolymerization of poly(ethylene terephthalate) wastes using ethanol and ethanol/water in supercritical conditions , 2006 .

[34]  I. Abdulagatov,et al.  (p, v, T, x) Measurements of {(1 − x)H2O + xC2H5OH} mixtures in the near-critical and supercritical regions , 2007 .

[35]  M. Poliakoff,et al.  Is it Possible to Achieve Highly Selective Oxidations in Supercritical Water? Aerobic Oxidation of Methylaromatic Compounds , 2004 .

[36]  Andrea Kruse,et al.  Hot compressed water as reaction medium and reactant properties and synthesis reactions , 2007 .