(Rs,1S)-N-(2-(tert-butyldimethylsilyloxy)-1-(4-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide

Base Information

Chemical Name:(Rs,1S)-N-(2-(tert-butyldimethylsilyloxy)-1-(4-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide
CAS No.:1312719-16-6
Molecular Formula:C₁₉H₃₂F₃NO₂SSi
Molecular Weight:423.615
Hs Code.:

Synonyms:(Rs,1S)-N-(2-(tert-butyldimethylsilyloxy)-1-(4-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide

Suppliers and Price of (Rs,1S)-N-(2-(tert-butyldimethylsilyloxy)-1-(4-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of (Rs,1S)-N-(2-(tert-butyldimethylsilyloxy)-1-(4-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of (Rs,1S)-N-(2-(tert-butyldimethylsilyloxy)-1-(4-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide

There total 4 articles about (Rs,1S)-N-(2-(tert-butyldimethylsilyloxy)-1-(4-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide 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: 81.0%

: 1312719-04-2
(Rs)-N-(2-(tert-butyldimethylsilyloxy)-1-(4-(trifluoromethyl)phenyl)ethylidene)-2-methylpropane-2-sulfinamide

: 1312719-16-6
(Rs,1S)-N-(2-(tert-butyldimethylsilyloxy)-1-(4-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide

Guidance literature:: (Rs)-N-(2-(tert-butyldimethylsilyloxy)-1-(4-(trifluoromethyl)phenyl)ethylidene)-2-methylpropane-2-sulfinamide; With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at -78 ℃; for 1h;

With water; In tetrahydrofuran; toluene; at -78 - 20 ℃; optical yield given as %de; diastereoselective reaction;
DOI:10.1016/j.tetasy.2011.01.011

Reference yield:

: 1312718-93-6
2-((tert-butyldimethylsilyl)oxy)-1-(4-(trifluoromethyl)phenyl)ethanone

: 1312719-16-6
(Rs,1S)-N-(2-(tert-butyldimethylsilyloxy)-1-(4-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: titanium(IV) isopropylate / tetrahydrofuran / Inert atmosphere; Reflux

2.1: diisobutylaluminium hydride / tetrahydrofuran; toluene / 1 h / -78 °C

2.2: -78 - 20 °C

With titanium(IV) isopropylate; diisobutylaluminium hydride; In tetrahydrofuran; toluene;
DOI:10.1016/j.tetasy.2011.01.011

Reference yield:

: 163089-34-7
N-methoxy-N-methyl-2-(1,1,2,2-tetramethyl-1-silapropoxy)acetamide

: 1312719-16-6
(Rs,1S)-N-(2-(tert-butyldimethylsilyloxy)-1-(4-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: magnesium; ethylene dibromide / tetrahydrofuran / 0.67 h / 20 °C / Inert atmosphere

1.2: 3 h / 0 °C / Inert atmosphere

2.1: titanium(IV) isopropylate / tetrahydrofuran / Inert atmosphere; Reflux

3.1: diisobutylaluminium hydride / tetrahydrofuran; toluene / 1 h / -78 °C

3.2: -78 - 20 °C

With titanium(IV) isopropylate; diisobutylaluminium hydride; magnesium; ethylene dibromide; In tetrahydrofuran; toluene;
DOI:10.1016/j.tetasy.2011.01.011