76159-32-5

Upstream product

• 123-75-1 pyrrolidine 
• 50-00-0 formaldehyd 
• 889-31-6 5,5-dimethyl-3-benzylamino-2-cyclohexen-1-one 
• 110-89-4 piperidine 
• 110-91-8 morpholine 
• 69370-88-3 3-Benzylamino-2-diethylaminomethyl-5,5-dimethyl-2-cyclohexen-1-on 
• 76159-25-6 3-Benzylamino-2-dimethylaminomethyl-5,5-dimethyl-2-cyclohexen-1-on 
• 76159-22-3 3-Benzylamino-5,5-dimethyl-2-(1-pyrrolidinylmethyl)-2-cyclohexen-1-on 
• 76159-21-2 3-Benzylamino-5,5-dimethyl-2-piperidinomethyl-2-cyclohexen-1-on 
• 76159-24-5 3-Benzylamino-5,5-dimethyl-2-morpholinomethyl-2-cyclohexen-1-on 
• 109-89-7 diethylamine 
• 124-40-3 dimethyl amine 
• 111-49-9 hexamethylene imine 

Downstream Products

• 309972-04-1 10-benzyl-3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione 

Relevant academic research and scientific papers

Synthesis of 9-R1-10-R-1,8-dioxo-decahydroacridines and dioximes based on them

3,3,6,6-Tetramethyl-9-R1-10-R-1,8- dioxo-1,2,3,4,5,6,7,8,9,10-decahydroacridines were synthesized through the intermediate α-R-methylenebisenamino ketones by the condensation of 5,5-dimethyl-3-N-R-aminocyclohex-2-enones with aliphatic, aromatic, and furan aldehydes (2-propanol, phosphorus pentoxide). It was found that the degree of substitution of the heterocycle in decahydroacridinediones has an effect on the direction of their transformations during oximation.

Participation of Vinylogous Carbonamide Groups Through the Generation of Carbiminium Compounds

Mercury EDTA dehydrogenation with Mannich bases derived from enaminones of dimedone and having a cyclic amine part mostly shows a neighbouring participation.From aromatically substituted vinylogous amides lactamamides are produced, while aliphatic substit