524741-03-5

Upstream product

• 186581-53-3 diazomethane 
• 91427-34-8 3-(2-Chlorophenyl)-3-methylbutansaeure 
• 479070-54-7 3-(2-Chlorophenyl)-2-cyano-3-methylbutansaeure-ethylester 
• 479070-55-8 3-(2-Chlorophenyl)-3-methylbutannitril 
• 694-80-4 2-bromo-1-chlorobenzene 

Downstream Products

• 479070-67-2 2-Chloro-6-(1,1-dimethyl-2-oxopropyl)benzoesaeure 
• 479070-53-6 4-(2-chlorophenyl)-2,4-dimethylpentan-2-ol 
• 479070-57-0 4-(2-chlorophenyl)-2-([2H₃]methyl)4-methyl[1,1,1-2H₃]pentan-2-ol 

Relevant academic research and scientific papers

On rearrangements by cyclialkylations of arylpentanols to 2,3-dihydro-1H-indene derivatives. Part 1. An unexpected rearrangement by the acid-catalyzed cyclialkylation of 4-(2-chlorophenyl)-2,4-dimethyl pentan-2-ol under formation of trans-4-chloro-2,3-dih

The acid-catalyzed cyclialkylation of 2,4-dimethyl-4-phenylpentan-2-ol led exclusively to the expected product, 2,3-dihydro-1,1,3,3-tetramethyl-1H-indene. However, analogous cyclialkylation of 4-(2-chlorophenyl)-2,4-dimethylpentan-2-ol (1) gave a ca. 1:1