tert-butyl N-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(3-methoxyphenyl)ethyl]-N-methylcarbamate

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Chemical Name:tert-butyl N-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(3-methoxyphenyl)ethyl]-N-methylcarbamate
CAS No.:1455472-25-9
Molecular Formula:C₂₅H₄₄N₂O₄Si
Molecular Weight:464.721
Hs Code.:

Synonyms:tert-butyl N-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(3-methoxyphenyl)ethyl]-N-methylcarbamate

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Chemical Property of tert-butyl N-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(3-methoxyphenyl)ethyl]-N-methylcarbamate

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Technology Process of tert-butyl N-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(3-methoxyphenyl)ethyl]-N-methylcarbamate

There total 7 articles about tert-butyl N-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(3-methoxyphenyl)ethyl]-N-methylcarbamate 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: 98.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 1455472-24-8
[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(3-methoxyphenyl)ethyl](methyl)amine

: 1455472-25-9
tert-butyl N-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(3-methoxyphenyl)ethyl]-N-methylcarbamate

Guidance literature:: With potassium carbonate; In tetrahydrofuran; at 0 - 25 ℃; for 16h;

Reference yield:

: 626-20-0
3-methoxystyrene

: 1455472-25-9
tert-butyl N-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(3-methoxyphenyl)ethyl]-N-methylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: AD-mix-α / water; tert-butyl alcohol / 16 h / 25 °C

2.1: chloro-trimethyl-silane / dichloromethane / 25 °C / Inert atmosphere

2.2: 1.5 h / 25 °C

2.3: 2 h / 25 °C

3.1: ethanol / 8 h / Reflux

3.2: 2 h / 0 - 25 °C

3.3: 16 h / 25 °C

4.1: potassium carbonate / tetrahydrofuran / 16 h / 0 - 25 °C

With chloro-trimethyl-silane; AD-mix-α; potassium carbonate; In tetrahydrofuran; ethanol; dichloromethane; water; tert-butyl alcohol;

Reference yield:

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

: 1455472-25-9
tert-butyl N-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(3-methoxyphenyl)ethyl]-N-methylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: ethanol / 8 h / Reflux

1.2: 2 h / 0 - 25 °C

1.3: 16 h / 25 °C

2.1: potassium carbonate / tetrahydrofuran / 16 h / 0 - 25 °C

With potassium carbonate; In tetrahydrofuran; ethanol;