(S)-2-((3S)-3-((tert-butyldimethylsilyl)oxy)pyrrolidin-1-yl)-1-(3,5-dimethylphenyl)ethanol

Base Information

Chemical Name:(S)-2-((3S)-3-((tert-butyldimethylsilyl)oxy)pyrrolidin-1-yl)-1-(3,5-dimethylphenyl)ethanol
CAS No.:1455472-60-2
Molecular Formula:C₂₀H₃₅NO₂Si
Molecular Weight:349.589
Hs Code.:

Synonyms:(S)-2-((3S)-3-((tert-butyldimethylsilyl)oxy)pyrrolidin-1-yl)-1-(3,5-dimethylphenyl)ethanol

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Chemical Property of (S)-2-((3S)-3-((tert-butyldimethylsilyl)oxy)pyrrolidin-1-yl)-1-(3,5-dimethylphenyl)ethanol

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Technology Process of (S)-2-((3S)-3-((tert-butyldimethylsilyl)oxy)pyrrolidin-1-yl)-1-(3,5-dimethylphenyl)ethanol

There total 6 articles about (S)-2-((3S)-3-((tert-butyldimethylsilyl)oxy)pyrrolidin-1-yl)-1-(3,5-dimethylphenyl)ethanol 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: 56.0%

: (2S)-2-(3,5-dimethylphenyl)oxirane

: 207113-36-8
(S)-3-((tert-butyldimethylsilyl)oxy)pyrrolidine

: 1455472-60-2
(S)-2-((3S)-3-((tert-butyldimethylsilyl)oxy)pyrrolidin-1-yl)-1-(3,5-dimethylphenyl)ethanol

Guidance literature:: In ethanol; at 80 ℃;

Reference yield:

: 1455472-59-9
(1S)-2-bromo-1-(3,5-dimethylphenyl)ethan-1-ol

: 1455472-60-2
(S)-2-((3S)-3-((tert-butyldimethylsilyl)oxy)pyrrolidin-1-yl)-1-(3,5-dimethylphenyl)ethanol

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / methanol / 0 °C

2: ethanol / 80 °C

With potassium carbonate; In methanol; ethanol;

Reference yield:

: 5379-16-8
3,5-dimethylacetophenone

: 1455472-60-2
(S)-2-((3S)-3-((tert-butyldimethylsilyl)oxy)pyrrolidin-1-yl)-1-(3,5-dimethylphenyl)ethanol

Guidance literature:: Multi-step reaction with 4 steps

1: sulfuric acid; acetic acid; N-Bromosuccinimide / 3.5 h / 0 - 20 °C / Inert atmosphere

2: 3,3-diphenyl-1-methylpyrrolidino[1,2-c]-1,3,2-oxazaborole; borane N,N-diethylaniline complex; tert-butyl methyl ether / 4 h / 40 °C / Inert atmosphere

3: potassium carbonate / methanol / 0 °C

4: ethanol / 80 °C

With N-Bromosuccinimide; borane N,N-diethylaniline complex; 3,3-diphenyl-1-methylpyrrolidino[1,2-c]-1,3,2-oxazaborole; tert-butyl methyl ether; sulfuric acid; potassium carbonate; acetic acid; In methanol; ethanol;