23740-63-8

Upstream product

• 2981-10-4 1-(cyclohex-1-en-1-yl)piperidine 
• 110-89-4 piperidine 

Downstream Products

• 86770-62-9 4a,5,6,7,8,8a-hexahydro-3-methyl-8-oxo-8a-(1-piperidinyl)-4-phenyl-4H-1,2-benzoxazine N-oxide 
• 58697-08-8 iodure de methyl piperidinio-2 cyclohexene-2 one 
• 16807-60-6 3-methoxycyclohex-2-en-1-one 
• 86770-65-2 2S-(2α,3α,3aα,6aα)-hexahydro-2-methyl-2-nitro-3-phenyl-6a-(1-piperidinyl)-1(2H)-pentalenone 

Relevant academic research and scientific papers

Studies on the Oxidation of Enamines with Molecular Oxygen. I. Oxidation of Some Piperidino Alkenes

In the autoxidation of 1-piperidinocyclohex-1-ene (1), 1-piperidinobut-1-ene (2), 3-piperidinopent-2-ene (3), and 1-piperidino-2-methyl-prop-1-ene (4) only products of an oxidative attack at the C=C-double bond are formed.Both α-aminoketones, the products of the rearrangement of primarily formed epoxides, and products of the oxidative scission of the C=C double bond are obtained.As a side reaction some hydrolysis of the starting enamines takes place.This hydrolysis proves that some water must be formed during the enamine oxidation.