2-({2-[1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-1-trifluoromethyl-ethyl]-phenylselanyl}-phenyl-methyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol

Base Information

Chemical Name:2-({2-[1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-1-trifluoromethyl-ethyl]-phenylselanyl}-phenyl-methyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol
CAS No.:195516-40-6
Molecular Formula:C₂₅H₂₆F₁₂O₂SeSi
Molecular Weight:693.507
Hs Code.:

2-({2-[1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-1-trifluoromethyl-ethyl]-phenylselanyl}-phenyl-methyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol

Synonyms:2-({2-[1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-1-trifluoromethyl-ethyl]-phenylselanyl}-phenyl-methyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol

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Chemical Property of 2-({2-[1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-1-trifluoromethyl-ethyl]-phenylselanyl}-phenyl-methyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol

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Technology Process of 2-({2-[1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-1-trifluoromethyl-ethyl]-phenylselanyl}-phenyl-methyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol

There total 5 articles about 2-({2-[1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-1-trifluoromethyl-ethyl]-phenylselanyl}-phenyl-methyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol 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: 13.0%

: 684-16-2
Hexafluoroacetone

: 195516-38-2
benzyl 2-[1-(tert-butyldimethylsiloxy)-2,2,2-trifluoro-1-(trifluoromethyl)-ethyl]phenyl selenide

: 195516-40-6
2-({2-[1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-1-trifluoromethyl-ethyl]-phenylselanyl}-phenyl-methyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; 1.) -78 deg C, 20 min, 2.) -78 deg C, 30 min;
DOI:10.1039/a704277i

Reference yield:

: 69739-34-0
t-butyldimethylsiyl triflate

: 195516-40-6
2-({2-[1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-1-trifluoromethyl-ethyl]-phenylselanyl}-phenyl-methyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / Et₃N / CH₂Cl₂ / 1.) 0 deg C, 2.) 40 deg C, 1 d

2: 13 percent / LDA / tetrahydrofuran / 1.) -78 deg C, 20 min, 2.) -78 deg C, 30 min

With triethylamine; lithium diisopropyl amide; In tetrahydrofuran; dichloromethane;
DOI:10.1039/a704277i

Reference yield:

: 70091-67-7
lithium 1,1,1,3,3,3-hexafluoro-2-(2-lithiophenyl)-2-propoxide

: 195516-40-6
2-({2-[1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-1-trifluoromethyl-ethyl]-phenylselanyl}-phenyl-methyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol

Guidance literature:: Multi-step reaction with 3 steps

2: 88 percent / Et₃N / CH₂Cl₂ / 1.) 0 deg C, 2.) 40 deg C, 1 d

3: 13 percent / LDA / tetrahydrofuran / 1.) -78 deg C, 20 min, 2.) -78 deg C, 30 min

With triethylamine; lithium diisopropyl amide; In tetrahydrofuran; dichloromethane;
DOI:10.1039/a704277i