3673-69-6

Upstream product

• 110-63-4 Butane-1,4-diol 
• 128-39-2 2,6-di-tert-butylphenol 

Downstream Products

• 39169-60-3 2-(3,5-di-tert-butyl-4-hydroxyphenyl)tetrahydrofuran 
• 125489-23-8 1-(3,5-di-tert-butyl-4-hydroxyphenyl)-4-hydroxy-1-butanone 
• 552314-65-5 4-(4-hydroxybutyl)-2-tert-butylphenol 
• 86223-05-4 4-(4-hydroxyphenyl)butanol 
• 99187-39-0 4-(4-hydroxyphenyl)butyl bromide 
• 125503-41-5 2,6-di-tert-butyl-4-(2-tetrahydrofurylidene)-2,5-cyclohexadienone 

Relevant academic research and scientific papers

Synthesis of 4-(ω-hydroxyalkyl)-2,6-di-tert-butylphenols and the properties of related sulfides

Reaction of 2,6-di-tert-butylphenol with aliphatic linear and branched diols in an alkaline medium at a temperature of 180-220°C leads to the formation of 4-(ω-hydroxyalkyl)-2,6-di-tert-butylphenols. The increase in the product yield and reducing the reaction temperature was reached at the catalysis of this reaction with zinc oxide. The structure of the diphenylalkane derivatives generated in side reaction was proved and the structural influence of the length of the aliphatic residue on the antioxidant effectiveness of the sulfides derived from the corresponding hydroxyalkylphenols was examined.

Alkylation of 2,6-di-tert-alkylphenols with alkanediols

There is a process disclosed for alkylating the nucleus of a phenol, said process comprising reacting an α, ωalkanediol containing from 3 to 8 carbon atoms with a phenol having an unsubstituted nuclear position para to the phenolic hydroxyl group; said ph