96682-22-3

Upstream product

• 4101-80-8 dichloroisoeverninic acid 
• 3465-63-2 4-Hydroxy-2-methoxy-6-methylbenzoesaeure-methylester 
• 72367-57-8 methyl 3,5-dichloro-4-hydroxy-2-methoxy-6-methylbenzoate 
• 39803-55-9 4-Benzyloxy-3,5-dichloro-2-hydroxy-6-methyl-benzoic acid methyl ester 
• 96682-20-1 methyl-4-benzyloxy-3,5-dichloro-2-methoxy-6-methylbenzoate 
• 96682-21-2 4-benzyloxy-3,5-dichloro-2-methoxy-6-methylbenzoic acid 
• 100-39-0 benzyl bromide 
• 22375-05-9 methyl 4-benzyloxy-2-hydroxy-6-methylbenzoate 
• 103233-31-4 Methyl-2-methoxy-6-methyl-4-pivaloyloxy-benzoat 
• 103233-29-0 Methyl-2-hydroxy-6-methyl-4-pivaloyloxy-benzoat 
• 3187-58-4 methyl orsellinate 
• 100-44-7 benzyl chloride 
• 103233-35-8 Methyl-3,5-dichlor-2-methoxy-6-methyl-4-pivaloyloxy-benzoat 
• 103233-34-7 Methyl-3,5-dichlor-2-hydroxy-6-methyl-4-pivaloyloxy-benzoat 

Relevant academic research and scientific papers

Improved Synthesis of Dichloroisoeverninic Acid

The Dichlorination of methyl isoeverninate 7a gave the geminal dichloroketone 12 as the major product.The title compound 1 was therefore synthesized via dichlorination of 4-protected methyl orsellinate 5a using the pivaloyloxy-function as a new protecting group in resorcyclic acids chemistry. - Keywords: 3,5-Dichloro-4-hydroxy-2-methoxy-6-methylbenzoic Acid, Dichloroisoeverninic Acid