C₂₆H₄₄O₄Si

Base Information

Chemical Name:C₂₆H₄₄O₄Si
CAS No.:1301726-07-7
Molecular Formula:C₂₆H₄₄O₄Si
Molecular Weight:448.718
Hs Code.:

C<sub>26</sub>H<sub>44</sub>O<sub>4</sub>Si

Synonyms:C₂₆H₄₄O₄Si

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Chemical Property of C₂₆H₄₄O₄Si

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Technology Process of C₂₆H₄₄O₄Si

There total 4 articles about C₂₆H₄₄O₄Si 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:

: C₂₀H₃₈O₃Si

: 1301726-07-7
C₂₆H₄₄O₄Si

Guidance literature:: Multi-step reaction with 4 steps

1: potassium osmate(VI) dihydrate; methanesulfonamide; water; potassium carbonate; 4-[(R)-[(2R,4R,5S)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxy-4-quinolinyl)methoxy]-1-[(R)-[(2R,4S,5R)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxy-4-quinolinyl)methoxy]phthalazine; potassium hexacyanoferrate(III) / tert-butyl alcohol / 22 h / 0 - 10 °C

2: lithium borohydride; water / tetrahydrofuran

3: sodium hydride; 1-[(2,4,6-triisopropylphenyl)sulfonyl]-1H-imidazole / tetrahydrofuran / 0 °C

4: tetrahydrofuran / 0 - 20 °C

With potassium osmate(VI) dihydrate; lithium borohydride; methanesulfonamide; water; sodium hydride; potassium carbonate; 4-[(R)-[(2R,4R,5S)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxy-4-quinolinyl)methoxy]-1-[(R)-[(2R,4S,5R)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxy-4-quinolinyl)methoxy]phthalazine; potassium hexacyanoferrate(III); 1-[(2,4,6-triisopropylphenyl)sulfonyl]-1H-imidazole; In tetrahydrofuran; tert-butyl alcohol; 1: Sharpless dihydroxylation / 3: Fraser-Reid epoxidation;
DOI:10.1016/j.tetlet.2010.11.013

Reference yield:

: 1301725-94-9
C₁₈H₃₈O₄Si

: 1301726-07-7
C₂₆H₄₄O₄Si

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydride; 1-[(2,4,6-triisopropylphenyl)sulfonyl]-1H-imidazole / tetrahydrofuran / 0 °C

2: tetrahydrofuran / 0 - 20 °C

With sodium hydride; 1-[(2,4,6-triisopropylphenyl)sulfonyl]-1H-imidazole; In tetrahydrofuran; 1: Fraser-Reid epoxidation;
DOI:10.1016/j.tetlet.2010.11.013

Reference yield:

: 1301725-93-8
C₂₀H₄₀O₅Si

: 1301726-07-7
C₂₆H₄₄O₄Si

Guidance literature:: Multi-step reaction with 3 steps

1: lithium borohydride; water / tetrahydrofuran

2: sodium hydride; 1-[(2,4,6-triisopropylphenyl)sulfonyl]-1H-imidazole / tetrahydrofuran / 0 °C

3: tetrahydrofuran / 0 - 20 °C

With lithium borohydride; water; sodium hydride; 1-[(2,4,6-triisopropylphenyl)sulfonyl]-1H-imidazole; In tetrahydrofuran; 2: Fraser-Reid epoxidation;
DOI:10.1016/j.tetlet.2010.11.013