4074-46-8

Upstream product

• 938-45-4 2-propionyl-p-cresol 
• 53889-94-4 4-methyl-2-(prop-1-enyl)phenol 
• 116436-12-5 4-methyl-2-propyl-aniline 
• 854260-67-6 allyl-(4-methyl-2-propyl-phenyl)-ether 
• 6628-06-4 2-allyl-4-methylphenol 
• 91329-58-7 3,3-Dichlor-1-(2-hydroxy-5-methyl-phenyl)-propen-⁽²⁾-on-⁽¹⁾ 
• 64-67-5 diethyl sulfate 
• 6738-23-4 2,4-dimethylanisole 
• 7647-01-0 hydrogenchloride 
• 64-17-5 ethanol 
• 116530-92-8 Opt_.-inakt. 4-Hydroxy-1-methyl-3-propyl-cyclohexan 
• 71-43-2 benzene 
• 104-93-8 p-methylanizole 
• 23431-48-3 allyl p-tolyl ether 

Downstream Products

• 26509-49-9 4-methyl-2,6-dibutyrylphenol 
• 26509-48-8 4-Hydroxy-1-methyl-5-propyl-3-allyl-benzol 
• 5397-51-3 allyl-(4-methyl-2,6-dipropyl-phenyl)-ether 
• 854260-67-6 allyl-(4-methyl-2-propyl-phenyl)-ether 

Relevant academic research and scientific papers

Catalytic alkylation of cresols with propanol-1

Study of the reaction of alkylation of ortho-, meta-, and para-cresols with propanol-1 in the presence of ferrite cobalt and manganese catalysts is reported. The effect of the catalyst composition and reaction conditions on the yield and isomeric composit

A New Rearrangement of Alkoxybenzyl Anions

Alkyl groups migrate from oxygen to carbon in alkyl aryl ethers which have been metalated in benzylic positions. 2,6-Dimethylanisole provides a variety of 2,6-dialkylphenols and their ethers in 45-80percent yields.Rearrangement products are obtained in 10-30percent yields from other dimethylanisoles and from methylanisoles.The reactions appear to proceed, like Wittig rearrangements, by homolytic cleavage of the alkyl-oxygen bond followed by recombination of the resulting radical pair in a different way.The rearrangements can be avoided by using methyl ethers and working at or below room temperature.