74384-33-1

Upstream product

• 1245624-46-7 4-hydroxy-3-(4-methoxyphenyl)-8-methyl-2H-chromen-2-one 
• 95-48-7 ortho-cresol 
• 104-01-8 4-Methoxyphenylacetic acid 
• 74384-22-8 (4-Methoxy-phenyl)-acetic acid o-tolyl ester 

Relevant academic research and scientific papers

Microwave-assisted efficient synthesis of 2-hydroxydeoxybenzoins from the alkali degradation of readily prepared 3-aryl-4-.hydroxycoumarins in water

This paper describes an operationally simple, green and efficient approach for the synthesis of 2-hydroxydeoxybenzoins bearing diverse substituents from the microwave-assisted alkali degradation of 3-aryl- 4-hydroxycoumarins in water. The latter compounds

Fries Rearrangement of ortho- and para-Methoxy Phenyl Acetates. The formation of Ketoesters

During the Fries rearrangement of o- and p-methoxy phenyl acetates with AlCl3 in nitromethane at 20 deg C substitution occurs mainly in the p-position of the phenolic residue to yield p-acylphenols.Larger quantities of o-acylphenols are obtained only, if