66790-20-3

Upstream product

• 335-99-9 2,2,3,3,4,4,5,5,6,6,7,7-dodecafluoro-1-heptanol 
• 100-39-0 benzyl bromide 

Downstream Products

• 1310492-17-1 2-(7-(benzyloxy)-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoroheptyl)pyridine 
• 1310492-19-3 2-(7-(benzyloxy)-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoroheptyl)-4,5-dimethylthiazole 
• 1310492-04-6 1-(7-(benzyloxy)-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoroheptyl)-2-methoxybenzene 
• 1310492-07-9 1-(7-(benzyloxy)-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoroheptyl)-4-methylbenzene 
• 1310492-15-9 1-(7-(benzyloxy)-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoroheptyl)-4-bromobenzene 
• 1310492-13-7 4-(7-(benzyloxy)-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoroheptyl)biphenyl 
• 1310492-23-9 ethyl 2-(7-(benzyloxy)-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoroheptyl)benzoate 
• 1310492-11-5 1-(7-(benzyloxy)-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoroheptyl)-3-(trifluoromethyl)benzene 
• 1310492-21-7 8-(7-(benzyloxy)-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoroheptyl)-1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione 
• 1310492-08-0 1-(7-(benzyloxy)-1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoroheptyl)-3-trifluoromethoxy benzene 

Relevant academic research and scientific papers

Copper-catalyzed arylation of 1 H-perfluoroalkanes

A general method has been developed for arylation of readily available 1H-perfluoroalkanes. The method employs aryl iodide and 1H-perfluoroalkane reagents, DMPU solvent, TMP2Zn base, and a copper chloride/phenanthroline catalyst. Preliminary mechanistic studies are reported.