2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(4-(trifluoromethyl)benzyl)amino)ethanol

Base Information

Chemical Name:2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(4-(trifluoromethyl)benzyl)amino)ethanol
CAS No.:1437124-95-2
Molecular Formula:C₁₈H₃₀F₃NO₂Si
Molecular Weight:377.522
Hs Code.:

Synonyms:2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(4-(trifluoromethyl)benzyl)amino)ethanol

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Chemical Property of 2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(4-(trifluoromethyl)benzyl)amino)ethanol

Chemical Property:

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Technology Process of 2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(4-(trifluoromethyl)benzyl)amino)ethanol

There total 3 articles about 2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(4-(trifluoromethyl)benzyl)amino)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: 66.0%

: 1402005-01-9
2-((2-((tert-butyldimethylsilyl)oxy)ethyl)amino)ethan-1-ol

: 402-49-3
4-bromomethyltrifluoromethylbenzene

: 1437124-95-2
2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(4-(trifluoromethyl)benzyl)amino)ethanol

Guidance literature:: With potassium carbonate; In acetonitrile; at 20 ℃;

Reference yield:

: 86864-60-0
2-(tert-butyldimethylsilyloxy)ethyl bromide

: 1437124-95-2
2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(4-(trifluoromethyl)benzyl)amino)ethanol

Guidance literature:: Multi-step reaction with 2 steps

1: acetonitrile / 1 h / Reflux

2: potassium carbonate / acetonitrile / 20 °C

With potassium carbonate; In acetonitrile;

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 1437124-95-2
2-((2-((tert-butyldimethylsilyl)oxy)ethyl)(4-(trifluoromethyl)benzyl)amino)ethanol

Guidance literature:: Multi-step reaction with 3 steps

1: 1H-imidazole / dichloromethane / 20 °C

2: acetonitrile / 1 h / Reflux

3: potassium carbonate / acetonitrile / 20 °C

With 1H-imidazole; potassium carbonate; In dichloromethane; acetonitrile;