73903-22-7

Upstream product

• 3213-28-3 3,5-dimethoxyphenethylamine 
• 407-25-0 trifluoroacetic anhydride 

Downstream Products

• 73903-23-8 N-<2-(2-Formyl-3,5-dimethoxyphenyl)athyl>-trifluoracetamid 
• 1332523-77-9 (Z)-3-{4,6-dimethoxy-2-[2-(trifluoroacetylamino)ethyl]phenyl}prop-2-enol 
• 1332523-76-8 3-{4,6-dimethoxy-2-[2-(trifluoroacetylamino)ethyl]phenyl}prop-2-ynol 
• 1332523-75-7 1-iodo-4,6-dimethoxy-2-[2-(trifluoroacetylamino)ethyl]-benzene 
• 1332523-71-3 ethenyl (Z)-3-{4,6-dimethoxy-2-[2-(trifluoroacetylamino)-ethyl]phenyl}prop-2-enyl carbonate 
• 73903-30-7 8-Methoxy-2-methyl-1,2,3,4-tetrahydroisochinolin 

Relevant academic research and scientific papers

30. Eine neue Synthese von 8-Hydroxy-2-methyl-1,2,3,4-tetrahydroisochinolin

Vilsmeier formylation of N--trifluoroacetamide (5) yielded the aldehyde 6, which under mild basic conditions was hydrolyzed to 7 and cyclized to 6,8-dimethoxy-3,4-dihydroisoquinoline (3).Methylation of 3 and reduction of the