58245-77-5

Upstream product

• 147088-65-1 6,6-Dimethoxy-4-methyl-cyclohexa-2,4-dienone 
• 67-63-0 isopropyl alcohol 
• 67-56-1 methanol 
• 93-51-6 2-Methoxy-4-methylphenol 

Relevant academic research and scientific papers

1,3-Methoxy rearrangement of masked o-benzoquinones: A novel synthesis of p-quinol ethers

(Chemical Equation Presented) p-Quinol ethers are valuable synthons in synthetic organic chemistry. MOBs 1a-1l can be converted to p-quinol ethers 2a-2i in a highly efficient manner via 1,3-methoxy migration catalyzed by Lewis acids. The migration was fou

Bromide-assisted oxidation of substituted phenols with hydrogen peroxide to the corresponding p-quinol and p-quinol ethers over WO4 2--exchanged layered double hydroxides

A simple and efficient one-pot synthesis of p-quinols and their ethers occurs over tungstate-exchanged layered double hydroxides (WO4 2--LDHs), which catalyze the bromide-assisted oxidation of substituted phenols to the corresponding 4-alkoxy- and 4-hydroxycyclohexa-2,5- dienones in high yields (see scheme).