(E)-3-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)prop-1-en-1-yl phenyl sulfone

Base Information

Chemical Name:(E)-3-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)prop-1-en-1-yl phenyl sulfone
CAS No.:1338566-16-7
Molecular Formula:C₃₈H₅₀O₇SSi
Molecular Weight:678.962
Hs Code.:

Synonyms:(E)-3-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)prop-1-en-1-yl phenyl sulfone

Suppliers and Price of (E)-3-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)prop-1-en-1-yl phenyl sulfone

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (E)-3-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)prop-1-en-1-yl phenyl sulfone

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (E)-3-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)prop-1-en-1-yl phenyl sulfone

There total 9 articles about (E)-3-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)prop-1-en-1-yl phenyl sulfone 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:

: 17872-92-3
(phenylsulfonylmethyl)trimethylsilane

: 1338566-14-5
2-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)acetoaldehyde

: 1338566-15-6
(Z)-3-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)prop-1-en-1-yl phenyl sulfone

: 1338566-16-7
(E)-3-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)prop-1-en-1-yl phenyl sulfone

Guidance literature:: (phenylsulfonylmethyl)trimethylsilane; With n-butyllithium; In 1,2-dimethoxyethane; hexane; at -80 ℃; for 0.5h; Inert atmosphere;

2-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)acetoaldehyde; In 1,2-dimethoxyethane; hexane; at -80 - 20 ℃; for 1.5h; optical yield given as %de; Inert atmosphere;
DOI:10.1021/ol202467z

Reference yield:

: 632354-40-6
(2S,3R,5S,6R)-5-benzyloxy-6-benzyloxymethyl-2-hydroxymethyltetrahydropyran-3-ol

: 1338566-15-6
(Z)-3-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)prop-1-en-1-yl phenyl sulfone

: 1338566-16-7
(E)-3-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)prop-1-en-1-yl phenyl sulfone

Guidance literature:: Multi-step reaction with 9 steps

1: trifluoromethylsulfonic anhydride; 2,6-dimethylpyridine / dichloromethane / Inert atmosphere

2: n-butyllithium / tetrahydrofuran / Inert atmosphere

3: tetrabutyl ammonium fluoride / tetrahydrofuran / Inert atmosphere

4: 4-methyl-morpholine / dichloromethane / Inert atmosphere

5: sodium hydrogencarbonate; methyl iodide; water / [D₃]acetonitrile / Inert atmosphere

6: samarium diiodide / tetrahydrofuran; methanol / 0 °C / Inert atmosphere

7: 2,6-dimethylpyridine / dichloromethane / 0 °C / Inert atmosphere

8: diisobutylaluminium hydride / dichloromethane / -78 °C / Inert atmosphere

9: n-butyllithium / 1,2-dimethoxyethane / -78 - 20 °C / Inert atmosphere

With 4-methyl-morpholine; 2,6-dimethylpyridine; n-butyllithium; samarium diiodide; trifluoromethylsulfonic anhydride; tetrabutyl ammonium fluoride; water; diisobutylaluminium hydride; sodium hydrogencarbonate; methyl iodide; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; dichloromethane; [D₃]acetonitrile; 9: |Peterson Olefination;
DOI:10.1021/jo302267f

Reference yield:

: 1338566-12-3
ethyl ((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-hydroxyoctahydropyrano[3,2-b]pyran-2-yl)acetate

: 1338566-15-6
(Z)-3-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)prop-1-en-1-yl phenyl sulfone

: 1338566-16-7
(E)-3-((2S,3R,4aS,6R,7S,8aR)-7-(benzyloxy)-6-((benzyloxy)methyl)-3-(t-butyldimethylsiloxy)octahydropyrano[3,2-b]pyran-2-yl)prop-1-en-1-yl phenyl sulfone

Guidance literature:: Multi-step reaction with 3 steps

1: 2,6-dimethylpyridine / dichloromethane / 0 °C / Inert atmosphere

2: diisobutylaluminium hydride / dichloromethane / -78 °C / Inert atmosphere

3: n-butyllithium / 1,2-dimethoxyethane / -78 - 20 °C / Inert atmosphere

With 2,6-dimethylpyridine; n-butyllithium; diisobutylaluminium hydride; In 1,2-dimethoxyethane; dichloromethane; 3: |Peterson Olefination;
DOI:10.1021/jo302267f