1246431-45-7

Upstream product

• 67-56-1 methanol 
• 212688-02-3 3,5-dibromo-4-hydroxyphenylacetic acid methyl ester 
• 14199-15-6 Methyl 4-hydroxyphenylacetate 

Downstream Products

• 1246431-47-9 C₁₈H₁₅Br₃O₆ 

Relevant academic research and scientific papers

Synthesis of (+)-O-methylthalibrine by employing a stereocontrolled Bischler-Napieralski reaction and an electrochemically generated diaryl ether

An efficient electrochemical four-step route was developed for the preparation of diaryl ether derivatives by using halogenation and dehalogenation processes in addition to electrochemical phenolic oxidation and reduction reactions. The synthesis of (+)-O

Electrochemical construction of the diaryl ethers: A synthetic approach to o-methylthalibrine

Electrochemical dimerization of halogenated p-hydroxyphenylacetic acid derivatives followed by Zn reduction provided the corresponding diaryl ethers. Manipulation of the reduction step using several procedures increased its efficiency, which enabled the construction of o-methylthalibrine, an isoquinoline-class alkaloid.