906360-44-9

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 6859-99-0 3-hydroxypiperazine 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 220384-55-4 1-(p-toluenesulfonyl)-piperidin-3-one 
• 220384-68-9 1-(p-toluenesulfonyl)-piperidin-3-ol 

Downstream Products

• 344257-61-0 3-(4-methoxyphenyl)-1-propylpiperidine 
• 19725-26-9 3-(4-methoxyphenyl)-piperidinehydrochloride 
• 906360-23-4 3-(4-methoxyphenyl)-1-p-toluenesulfonylpiperidine 

Relevant academic research and scientific papers

Concise synthesis of 3-arylpiperidines

We present an easy and straightforward synthesis of 3-arylpiperidines by Grignard addition of piperidin-3-one with different arylmagnesium bromide reagents and acidic dehydroxylation of the resulting tertiary alcohol with the combination of triethylsilane and boron trifluoride etherate. This facile strategy was further used to synthesize preclamol. A highly regioselective dehydration of 3-arylpiperidin-3-ol with boron trifluoride etherate was investigated for preparing 3-aryl-1,4,5,6-tetrahydropyridine skeleton. A novel selenium dioxide mediated dihydroperoxidation of 3-aryl-1,4,5,6-tetrahydropyridine was also examined.