94102-96-2

Upstream product

• 94102-95-1 5-bromo-2-nitro-3-propylphenol 
• 74-88-4 methyl iodide 
• 621-27-2 3-n-propylphenol 
• 55789-02-1 α-ethyl-3-hydroxybenzyl alcohol 
• 100-83-4 meta-hydroxybenzaldehyde 
• 94102-91-7 2,4,5,6-tetrabromo-3-propylphenol 
• 94102-92-8 3-bromo-5-propylphenol 
• 1700-37-4 3-Benzyloxybenzaldehyde 

Downstream Products

• 94103-04-5 methyl 2-methoxy-4-(5-methoxy-4-nitro-3-propylphenoxy)-6-pentylbenzoate 
• 94103-05-6 methyl 5-bromo-4-(5-methoxy-4-nitro-3-propylphenoxy)-2-methoxy-6-pentylbenzoate 
• 94103-09-0 methyl 5-iodo-4-(5-methoxy-4-nitro-3-propylphenoxy)-2-methoxy-6-pentylbenzoate 
• 94103-10-3 methyl 5-iodo-4-(2-iodo-5-methoxy-4-nitro-3-propylphenoxy)-2-methoxy-6-pentylbenzoate 

Relevant academic research and scientific papers

Naturally Occurring Dibenzofurans. Part 6. Synthesis of Didymic Acid

The synthesis of the lichen dibenzofuran didymic acid (1) (3-hydroxy-7-methoxy-1-pentyl-9-propyldibenzofuran-2-carboxylic acid) by intramolecular Ullmann coupling of methyl 5-bromo-4-(2-bromo-5-methoxy-3-propylphenoxy)-2-methoxy-6-pentylbenzoate (34) and methyl 5-iodo-4-(2-iodo-5-methoxy-4-nitro-3-propylphenoxy)-2-methoxy-6-pentylbenzoate (32) and appropriate further transformations, is described.