426823-89-4

Upstream product

• 95-74-9 3-chloro-p-toluidine 
• 426824-19-3 2-(1-acetyl-3,3,3-trichloropropyl)-3-hydroxy-5,5-dimethylcyclohex-2-en-1-one 
• 56686-56-7 3,5,5,5-tetrachloro-2-pentanone 
• 126-81-8 dimedone 

Relevant academic research and scientific papers

A new method for the synthesis of N-substituted (4-oxo-4,5,6,7-tetrahydroindol-3-yl)acetic acids

A new method for the synthesis of N-substituted 2-(4-oxo-4,5,6,7-tetrahydroindol-3-yl)acetic acids was developed. Alkylation of cyclic 1,3-diketones with 3,5,5,5-tetrachloropentan-2-one affords 1,4-diketones, which undergo cyclization with different primary amines into N-substituted 3-(2,2,2-trichloroethyl)-4,5,6,7-tetrahydroindol-4-ones. Acid hydrolysis of the latter gives the corresponding indol-3-ylacetic acids. The structures of the compounds obtained were confirmed by 1H and 13C NMR data.