105230-46-4

Upstream product

• 19262-74-9 p-ethyl benzoate diazonium salt 
• 70-55-3 toluene-4-sulfonamide 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 94-09-7 p-aminoethylbenzoate 
• 51934-41-9 4-iodobenzoic acid ethyl ester 
• 111017-08-4 ethyl 4-[bis(trimethylsilyl)amino]benzoate 

Downstream Products

• 680983-41-9 ethyl 4-[(4-cyanophenyl)amino]-benzoate 
• 112033-48-4 ethyl 4-(cyclopropylamino)benzoate 
• 458550-44-2 ethyl 4-[(4-bromophenyl)amino]-benzoate 
• 55791-74-7 4-octylamino-benzoic acid ethyl ester 
• 75681-67-3 4-pentylamino-benzoic acid ethyl ester 
• 102004-72-8 4-cyclohexylamino-benzoic acid ethyl ester 
• 909709-18-8 4-cyclopentylamino-benzoic acid ethyl ester 
• 3757-99-1 p-Methylseleno-benzoesaeureethylester 

Relevant academic research and scientific papers

A general animation method based on the addition of polyfunctional arylmagnesium reagents to functionalized arylazo tosylates

A one-pot reaction sequence consisting of a Grignard reaction, allylation, and reduction provides new functionalized diarylamines in good yields (see scheme, Ts = toluene-4-sulfonyl, NMP = N-methylpyrrolidine, TFA = trifluoroacetic acid). In the first ste

General preparation of primary, secondary, and tertiary aryl amines by the oxidative coupling of polyfunctional aryl and heteroaryl amidocuprates

(Chemical Equation Presented). A tolerant reaction: Functionalized tertiary amines have been prepared by the oxidative coupling of amidocuprates with chloranil used as the oxidant (see Scheme). A high tolerance of functional groups and insensitivity to steric hindrance characterize this general amination reaction.