30784-29-3

Upstream product

• 860532-09-8 4-(2-methylheptan-2-yl)aniline 
• 625-25-2 2-Methyl-2-heptanol 
• 108-95-2 phenol 
• 7446-70-0 aluminium trichloride 
• 16252-11-2 (2-methylheptan-2-yl)benzene 
• 859977-47-2 2-methyl-2-(4-nitro-phenyl)-heptane 
• 71-43-2 benzene 
• 15870-10-7 2-methylhept-1-ene 

Downstream Products

• 851231-28-2 trifluoro-methanesulfonic acid 4-(1,1-dimethyl-hexyl)-phenyl ester 
• 851231-33-9 2-[4-(1,1-dimethyl-hexyl)-phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane 
• 851231-37-3 1-bromo-4-(1,1-dimethylhexyl)benzene 
• 56823-81-5 p-t-octylphenyl 3-(5-t-butyl-2,3-dimethyl-4-hydroxyphenyl)propionate 

Relevant academic research and scientific papers

ALKYLATION OF HYDROXYARENES WITH OLEFINS, ALCOHOLS AND ETHERS IN IONIC LIQUIDS

Hydroxyarenes are alkylated using an ionic liquid catalyst system with olefins, alcohols, or ethers as alkylating agents. The ionic liquid catalyst system comprises chloroindate (III) anions. The reactions may be conducted at moderate temperatures and pressures to yield commercially relevant alkylated hydroxyarene compounds.

Process for treating 2-ethylhexyl p-methoxycinnamate in the presence of a phenol

A process for treating 2-ethylhexyl p-methoxycinnamic acid ester is described. The process comprises heating, preferably distilling, the ester in the presence of a phenol to insure that the ester is considered Ames negative.