2-(tert-butyldiMethylsilyl )oxyl alcohol trifluorin Methanesulfonate

2-(tert-butyldiMethylsilyl )oxyl alcohol trifluorin Methanesulfonate Basic information
Product Name:2-(tert-butyldiMethylsilyl )oxyl alcohol trifluorin Methanesulfonate
Synonyms:Trifluoromethanesulfonic acid 2-[[(tert-butyl)dimethylsilyl]oxy]ethyl ester;2-(t-ButyldiMethylsilyl)oxyethyl triflate;Methanesulfonicacid,1,1,1-trifluoro-,2-[[(1,1-diMethylethyl)diMethylsilyl]oxy]ethylester;2-(t-Butyldimethylsilyloxy)EthylTrifluoromethanesulfonate;2-(tert-butyldiMethylsilyl )oxyl alcohol trifluorin Methanesulfonate;2-(tert-butyldiMethylsilyloxy)ethyl trifluoroMethanesulfonate;1,1,1-Trifluoromethanesulfonic acid 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethyl ester;2-{[Dimethyl(2-methyl-2-propanyl)silyl]oxy}ethyl trifluoromethanesulfonate
CAS:164162-36-1
MF:C9H19F3O4SSi
MW:308.39
EINECS:
Product Categories:
Mol File:164162-36-1.mol
2-(tert-butyldiMethylsilyl )oxyl alcohol trifluorin Methanesulfonate Structure
2-(tert-butyldiMethylsilyl )oxyl alcohol trifluorin Methanesulfonate Chemical Properties
Boiling point 253℃
density 1.172
Fp 107℃
Safety Information
MSDS Information
2-(tert-butyldiMethylsilyl )oxyl alcohol trifluorin Methanesulfonate Usage And Synthesis
Uses2-(tert-butyldiMethylsilyl )oxyl alcohol trifluorin Methanesulfonate is used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.
Synthesis1.jpg
The reaction was carried out under a nitrogen atmosphere. TBS- ethylene glycol prepared as per step 1 (85.10g, 0.48 mol) and 2, 6-Lutidine (84.28ml, 0.72 mol) were stirred in n-heptane (425ml) to give a clear solution which was then cooled to -15 to - 25°C. Trifluoromethanesulfonic anhydride (Tf2O) (99.74 ml, 0.590 mol) was added drop-wise over a period of 45 minutes to the n-heptane solution (white precipitate starts to form immediately) while maintaining the reaction at -15 to -25°C. The reaction mixture was kept at temperature between -15 to -25°C for 2 hours. The precipitate generated was filtered off. The filtrate was then evaporated up to ~2 volumes with respect to TBS-ethyiene glycol (~200 ml).
2-(tert-butyldiMethylsilyl )oxyl alcohol trifluorin Methanesulfonate Preparation Products And Raw materials
Preparation Products40-O-[2-(t-butyldimethylsilyl)oxy]ethyl rapamycin
2,6-di-tert-butyl-4-methylene-2,5-cyclohexadienone Everolimus Ring-Opening Impurity Rapamycin Ethyleneglycol bistriflate Everolimus Related Compound 2 Methanesulfonic acid, trifluoro-, 2-hydroxyethyl ester EveroliMus iMpurity EveroliMus-d4 Everolimus Related Compound 3 Everolimus O-Ethyl Impurity Everolimus Impurity 1 BIS(T-BUTYLDIMETHYLSILOXY)ETHANE Everolimus

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