C₂₆H₃₈O₅Si

Base Information

Chemical Name:C₂₆H₃₈O₅Si
CAS No.:1431725-68-6
Molecular Formula:C₂₆H₃₈O₅Si
Molecular Weight:458.67
Hs Code.:

C<sub>26</sub>H<sub>38</sub>O<sub>5</sub>Si

Synonyms:C₂₆H₃₈O₅Si

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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 C₂₆H₃₈O₅Si

Chemical Property:

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Technology Process of C₂₆H₃₈O₅Si

There total 3 articles about C₂₆H₃₈O₅Si 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: 91.0%

: C₂₆H₃₆O₃Si

: 1431725-68-6
C₂₆H₃₈O₅Si

Guidance literature:: With methanesulfonamide; AD-mix-α; water; In tert-butyl alcohol; at 0 ℃; for 36h; stereoselective reaction;
DOI:10.1002/anie.201203406

Reference yield:

: 186641-79-2
(R)-4-((tert-Butyldiphenylsilyl)oxy)-3-methylbutanal

: 1431725-68-6
C₂₆H₃₈O₅Si

Guidance literature:: Multi-step reaction with 3 steps

1: dichloromethane / 18 h / 55 °C

2: pyridinium p-toluenesulfonate / benzene / 48 h / Reflux

3: water; AD-mix-α; methanesulfonamide / tert-butyl alcohol / 36 h / 0 °C

With methanesulfonamide; AD-mix-α; water; pyridinium p-toluenesulfonate; In dichloromethane; tert-butyl alcohol; benzene; 1: |Wittig Olefination / 3: |Sharpless Dihydroxylation;
DOI:10.1002/anie.201203406

Reference yield:

: C₂₄H₃₂O₂Si

: 1431725-68-6
C₂₆H₃₈O₅Si

Guidance literature:: Multi-step reaction with 2 steps

1: pyridinium p-toluenesulfonate / benzene / 48 h / Reflux

2: water; AD-mix-α; methanesulfonamide / tert-butyl alcohol / 36 h / 0 °C

With methanesulfonamide; AD-mix-α; water; pyridinium p-toluenesulfonate; In tert-butyl alcohol; benzene; 2: |Sharpless Dihydroxylation;
DOI:10.1002/anie.201203406