2,2-Difluoro-1-pentafluorophenyl-2-[1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoro-2-pentafluoroethyloxy-ethoxy)-ethoxy]-ethanone

Base Information

Chemical Name:2,2-Difluoro-1-pentafluorophenyl-2-[1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoro-2-pentafluoroethyloxy-ethoxy)-ethoxy]-ethanone
CAS No.:70627-98-4
Molecular Formula:C₁₄F₂₀O₄
Molecular Weight:612.12
Hs Code.:

Synonyms:2,2-Difluoro-1-pentafluorophenyl-2-[1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoro-2-pentafluoroethyloxy-ethoxy)-ethoxy]-ethanone

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Chemical Property of 2,2-Difluoro-1-pentafluorophenyl-2-[1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoro-2-pentafluoroethyloxy-ethoxy)-ethoxy]-ethanone

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Technology Process of 2,2-Difluoro-1-pentafluorophenyl-2-[1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoro-2-pentafluoroethyloxy-ethoxy)-ethoxy]-ethanone

There total 2 articles about 2,2-Difluoro-1-pentafluorophenyl-2-[1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoro-2-pentafluoroethyloxy-ethoxy)-ethoxy]-ethanone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 14.2%

: C₂F₅O(CF₂CF₂)2CF₂C(O)F

: 879-05-0
2,3,4,5,6-pentafluorophenylmagnesium bromide

: 2641-34-1
perfluoro-2,5-dimethyl-3,6-dioxanonanoyl fluoride

: 363-72-4
Pentafluorobenzene

: 70627-98-4
2,2-Difluoro-1-pentafluorophenyl-2-[1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoro-2-pentafluoroethyloxy-ethoxy)-ethoxy]-ethanone

: 70627-97-3
2,3,3,3-Tetrafluoro-2-(1,1,2,3,3,3-hexafluoro-2-heptafluoropropyloxy-propoxy)-1-pentafluorophenyl-propan-1-one

: 70640-77-6
2,2-Difluoro-1,1-bis-pentafluorophenyl-2-[1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoro-2-pentafluoroethyloxy-ethoxy)-ethoxy]-ethanol

Guidance literature:: In diethyl ether; at 0°C after 3.5 h only 25 % of C6F5MgBr reacted, then allowing the mixt. to warm to 20°C and stirring for another 48 h, hydrolysis;
DOI:10.1016/S0022-1139(00)82083-7