REFERENCES
- Hoffmann-La Roche Inc. Process for Preparing 2,4-Diamino-5-(substituted benzyl)-pyrimidines . US Patent 4,115,650 . Sep. 19, 1978 .
- Manchand , P.S. , Rosen , P. , Belica , P.S. , Oliva , G.V. , Perrotta , A.V. and Wong , H.S. 1992 . Synthesis of Antibacterial 2,4-Diamino-5-benzylpyrimidines. Ormetoprim and Trimethoprim . J. Org. Chem. , 57 ( 13 ) : 3531 – 3535 .
- Rao , D.V. and Stuber , F.A. 1983 . An Efficient Synthesis of 3,4,5-Trimethoxybenzaldehyde from Vanillin . Synthesis , : 308
- Kitajima , N. , Takemura , K. , Moro-oka , Y. , Yoshikuni , T. , Akada , M. , Tomotaki , Y. and Taniguchi , M. 1988 . The Selective Liquid-Phase Oxidation of 3,4,5-Trimethoxytoluene to 3,4,5-Trimethoxybenzaldehyde . Bull. Chem. Soc. Jpn. , 61 ( 3 ) : 1035 – 1037 .
- Manchand , P.S. , Belica , P.S. and Wong , H.S. 1990 . Synthesis of 3,4,5-Trimethoxybenzaldehyde . Synth. Commun. , 20 ( 17 ) : 2659 – 2666 .
- Lindley , J. 1984 . Copper-assisted Nucleophilic Substitution of Aryl Halogen . Tetrahedron , 40 ( 9 ) : 1433 – 1456 .
- Bebon-Rampal , C. and Vanhove , D. 1992 . Catalyseurs Supportés Pour l′ Alcoxylation de Molécules Aromatiques Substituées . Bull. Soc. Chim. Fr. , 129 ( 5 ) : 501 – 508 .
- Aalten , H.L. , van Koten , G. , Grove , D.M. , Kuilman , T. , Piekstra , O.G. , Hulshof , L.A. and Sheldon , R.A. 1989 . The Copper Catalysed Reaction of Sodium Methoxide with Aryl Bromides. A Mechanistic Study Leading to a Facile Synthesis of Anisole Derivatives . Tetrahedron , 45 ( 17 ) : 5565 – 5578 .
- de la Mare , P.B.D. and Newman , P.A. 1984 . Solvolytic Elimination and Hydrolysis Promoted by Aromatic Hydroxy Group. Part 1. The Reaction of 2,6-Dibromo-4-dibromomethylphenol and of 2,6-Dibromo-4-bromomethylenecyclohexa-2,5-dienone with Water in 95% 1,4-Dioxane . J. Chem. Soc., Perkin Trans. II , : 231 – 238 .
- de la Mare , P.B.D. and Newman , P.A. 1984 . Solvolytic Elimination and Hydrolysis Promoted by Aromatic Hydroxy Group. Part 2. The Hydrolysis of 2-Bromo-4-dibromomethylphenol in 95% 1,4-Dioxane . J. Chem. Soc., Perkin Trans. II , : 1797 – 1802 .
- Cuprous Chloride Needed no Deterioration, Just as well Freshly Prepared
- Under our Work Conditions, Reaction Pressure was about 0.4 MPa