185034-25-7

Upstream product

• 2923-28-6 silver trifluoromethanesulfonate 
• 342573-87-9 4-(2,2-dimethylpropoxy)-2,3,5-trimethylbenzoic acid chloride 
• 185034-24-6 2-(2,2-Dimethyl-propoxy)-1,3,4-trimethyl-benzene 
• 2346-07-8 neopentyl tosylate 
• 2416-94-6 2,3,6-trimethylphenol 

Relevant academic research and scientific papers

Changing the ortho/para ratio in aromatic acylation reactions by changing reaction conditions: A mechanistic explanation from kinetic measurements

Kinetic measurements of the acylation of toluene (2a) and p-xylene (2b), side-chain deuterated toluene (2a-d3), as well as perdeuterated toluene (2a-d8) and p-xylene (2b-d10) with the aroyl triflate 1 in 1,2-dichloroethane

The first unequivocal evidence of the reacting electrophile in aromatic acylation reactions

The acylation of aromatic compounds with aroyl triflates can be performed in organic solvents (1,2-dichloroethane) without Friedel-Crafts catalysts. These reaction conditions allow kinetic investigations of the reaction in homogeneous solution. From rate