Welcome to chemicalbook!
Chinese English Japanese Germany Korea
010-86108875
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

1402005-01-9

2-[[2-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]ethyl]amino]ethanol synthesis

4synthesis methods
86864-60-0 Synthesis
(2-BROMOETHOXY)-TERT-BUTYLDIMETHYLSILANE

86864-60-0
201 suppliers
$5.00/1g

2-[[2-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]ethyl]amino]ethanol

1402005-01-9
6 suppliers
inquiry

-

Yield:1402005-01-9 100%

Reaction Conditions:

in acetonitrile; for 3 h;Reflux;

Steps:

13; 6.1 Step 1. Preparation of 2-((2-((tert-butyldimethylsilyl)oxy)ethyl)amino)ethan-l-ol 51

A solution of ethanolamine (77 mL, 1.25 mol) and (2-bromoethoxy)-tert-butyl dimethylsilane (15 g, 62.7 mmol) in anhydrous acetonitrile (200 mL) was refluxed for 3 hours. Upon completion the reaction was cooled to room temperature, diluted with water (400 mL) and extracted with ethyl acetate (3 x 150 mL). The combined ethyl acetate extracts were dried on magnesium sulfate, filtered and concentrated in vacuo to dryness. The residue was purified by filtration through a pad of silica first with 50% ethyl acetate/hexanes then 50% MeOH/EtOAc to afford 51 as a pale yellow oil (14 g, 100%).

References:

WO2017/177326,2017,A1 Location in patent:Page/Page column 79-81

18162-48-6 Synthesis
tert-Butyldimethylsilyl chloride

18162-48-6
681 suppliers
$9.00/5g

2-[[2-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]ethyl]amino]ethanol

1402005-01-9
6 suppliers
inquiry