A new protocol for O-methylation of phenolic compounds with trimethyl phosphite or trimethyl phosphate under solvent-free condition and microwave irradiation

Phosphorus, Sulfur and Silicon and the Related Elements

Volumn 178, Issue 11, 2003, Pages 2343-2348

  Saidi, Mohammad R ^a   Rajabi, Fatemeh ^a  

^a SHARIF UNIVERSITY OF TECHNOLOGY   (Iran)

Author keywords

Alkyl aryl ethers; Microwave irradiation; Solvent free; Trimethyl phosphite

Indexed keywords

2 METHOXYNAPHTHALENE; 2 NAPHTHOL; COUMARIN DERIVATIVE; NAPHTHALENE DERIVATIVE; NAPHTHOL DERIVATIVE; PHENOL DERIVATIVE; PHOSPHITE; PHOSPHORUS DERIVATIVE; SOLVENT; TRIMETHYL PHOSPHATE; TRIMETHYLPHOSPHITE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; METHYLATION; MICROWAVE IRRADIATION; QUANTITATIVE ANALYSIS;

EID: 0344256698     PISSN: 10426507     EISSN: None     Source Type: Journal    
DOI: 10.1080/714040947     Document Type: Article

References (24)

1. S. Ouk, S. Thiebaud, E. Borredon, P. Legars, and L. Lecomte, Tetrahedron Lett., 43, 2661 (2002).
2. L. Henk, H. L. Aalten, G. Koten, et al., Tetrahedron, 45, 5565 (1989).
3. G. Dorothea, Phenol Derivatives. Ullmann's Encyclopedia of Industrial Chemistry, edited by E. Barbara, H. Stephen, and S. Gail (VCH, Weinheim, 1991), vol. A19.
4. a) F. Merger, F. Tovae, and L. Schroff, US Pat., 1980, 192, 949; CA, 92, 6229c (1980);
5. b) G. Barcelo, D. Grenouillat, J. P. Senet, and G. Sennyey, Tetrahedron, 46, 1839 (1990);
6. c) Y. Lee and I. Shimizu, Synlett, 1063 (1998).
7. a) N. Notari, F. Mizia, and F. Rivetti, US Pat., 1998, 849,955; CA, 129, 54182m (1998);
8. b) A. Perosa, M. Selva, P. Tondo, and F. Zordan, Synlet, 272 (2000).
9. a) P. Tundo and M. Selva, Chem. Tech., 25, 31 (1995);
10. b) M. Selva, F. Trotta, and P. J. Tundo, Chem. Soc., Perkin Trans., 2, 519 (1992).
11. a) R. A. Abramovitch, Org. Prep. Proc. Int., 23, 683 (1991);
12. b) D. M. P. Mingos and D. R. Baghurst, Chem. Soc. Rev., 20, 1 (1991);
13. c) K. D. Raner, C. R. Strauss, R. W. Trainor, and J. S. Thorn, J. Org. Chem., 60, 2456 (1995);
14. d) T. Cablewski, A. F. Faux, and C. R. Strauss, J. Org. Chem., 59, 3408 (1994).
15. a) M. R. Saidi and K. Bigdeli, J. Chem. Res. (S), 800 (1998);
16. b) A. Sharifi, M. M. Mojtahedi, and M. R. Saidi, Tetrahedron Lett., 40, 2661 (1999);
17. c) M. M. Mojtahedi, M. R. Saidi, M. M. Heravi, and M. Bolourtchian, Monash. Chem., 130, 1175 (1999);
18. d) M. R. Saidi, M. M. Mojtahedi, Sh. Kaamyabi, and M. Bolourtchian, J. Sciences, I. R. Iran, 11, 217 (2000);
19. e) M. M. Mojtahedi, M. R. Saidi, M. Bolourtchian, and M. M. Heravi, Phosphorus, Sulfur, and Silicon, 177, 289 (2002);
20. f) M. M. Mojtahedi, M. R. Saidi, J. S. Shirzi, and M. Bolourtchian, Synth. Commun., 32, 851 (2002);
21. g) M. M. Mojtahedi, A. Sharifi, Sh. Kaamyabi, and M. R. Saidi, J. Chem. Res.(S), 286 (2002).
22. M. R. Saidi, Indian J. Chem., 21B, 474 (1982).
23. a) Dictionary of Organic Compounds (Chapman and Hall; New York, 1982), vol. 4, p. 3704; vol. 3, p. 2999.
24. a) Dictionary of Organic Compounds (Chapman and Hall; New York, 1982), vol. 4, p. 3704; vol. 3, p. 2999.