Efficient and convenient synthesis of 3,4,5-trimethoxybenzaldehyde from p-cresol

Synthetic Communications

Volumn 32, Issue 18, 2002, Pages 2809-2814

  Ji, Ya Fei ^a   Zong, Zhi Min ^a   Wei, Xian Yong ^a  

^a CHINA UNIVERSITY OF MINING AND TECHNOLOGY   (China)

Author keywords

3,4,5 Trimethoxybenzaldehyde; Bromination; Hydrolysis; Methoxylation; Methylation; p Cresol

Indexed keywords

3,4,5 TRIMETHOXYBENZALDEHYDE; BENZALDEHYDE DERIVATIVE; PARA CRESOL; UNCLASSIFIED DRUG;

ARTICLE; BROMINATION; CHEMICAL MODIFICATION; DRUG SYNTHESIS; HYDROLYSIS; METHYLATION; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 0036041801     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120006464     Document Type: Article

References (12)

1. Synthesis of antibacterial 2,4-diamino-5-benzylpyrimidines. Ormetoprim and trimethoprim
2. An efficient synthesis of 3,4,5-trimethoxybenzaldehyde from vanillin
3. The selective liquid-phase oxidation of 3,4,5-trimethoxytoluene to 3,4,5-trimethoxybenzaldehyde
4. Synthesis of 3,4,5-trimethoxybenzaldehyde
5. Copper-assisted nucleophilic substitution of aryl halogen
6. Catalyseurs supportés pour 1 alcoxylation de molécules aromatiques substituées
7. The copper catalysed reaction of sodium methoxide with aryl bromides. A mechanistic study leading to a facile synthesis of anisole derivatives
8. 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
9. Solvolytic elimination and hydrolysis promoted by Aromatic Hydroxy Group. Part 2. The hydrolysis of 2-bromo-4-dibromomethylphenol in 95% 1,4-dioxane