(2S,3R)-3-(tert-butyldimethylsilanyloxy)-2-[3-(tert-butyldiphenylsilanyloxy)propoxy]hex-5-yn-1-ol

Base Information

Chemical Name:(2S,3R)-3-(tert-butyldimethylsilanyloxy)-2-[3-(tert-butyldiphenylsilanyloxy)propoxy]hex-5-yn-1-ol
CAS No.:1101134-08-0
Molecular Formula:C₃₁H₄₈O₄Si₂
Molecular Weight:540.891
Hs Code.:

Synonyms:(2S,3R)-3-(tert-butyldimethylsilanyloxy)-2-[3-(tert-butyldiphenylsilanyloxy)propoxy]hex-5-yn-1-ol

Suppliers and Price of (2S,3R)-3-(tert-butyldimethylsilanyloxy)-2-[3-(tert-butyldiphenylsilanyloxy)propoxy]hex-5-yn-1-ol

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

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Chemical Property of (2S,3R)-3-(tert-butyldimethylsilanyloxy)-2-[3-(tert-butyldiphenylsilanyloxy)propoxy]hex-5-yn-1-ol

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Technology Process of (2S,3R)-3-(tert-butyldimethylsilanyloxy)-2-[3-(tert-butyldiphenylsilanyloxy)propoxy]hex-5-yn-1-ol

There total 1 articles about (2S,3R)-3-(tert-butyldimethylsilanyloxy)-2-[3-(tert-butyldiphenylsilanyloxy)propoxy]hex-5-yn-1-ol 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:

: 1101134-07-9
C₄₁H₆₀O₅Si₃

: 1101134-08-0
(2S,3R)-3-(tert-butyldimethylsilanyloxy)-2-[3-(tert-butyldiphenylsilanyloxy)propoxy]hex-5-yn-1-ol

Guidance literature:: With methanol; potassium carbonate; at 0 - 20 ℃; for 16h; Inert atmosphere;
DOI:10.1016/j.tet.2010.05.028

Reference yield: 95.0%

: 1101134-08-0
(2S,3R)-3-(tert-butyldimethylsilanyloxy)-2-[3-(tert-butyldiphenylsilanyloxy)propoxy]hex-5-yn-1-ol

: 1101134-09-1
(2R,3R)-3-(tert-butyldimethylsilanyloxy)-2-[3-(tert-butyldiphenylsilyloxy)propoxy]hex-5-ynal

Guidance literature:: With sulfur trioxide pyridine complex; triethylamine; In dimethyl sulfoxide; at 0 - 20 ℃; for 4h; Inert atmosphere;
DOI:10.1016/j.tet.2010.05.028