C₃₂H₄₄O₅Si

Base Information

Chemical Name:C₃₂H₄₄O₅Si
CAS No.:1292808-54-8
Molecular Formula:C₃₂H₄₄O₅Si
Molecular Weight:536.784
Hs Code.:

C<sub>32</sub>H<sub>44</sub>O<sub>5</sub>Si

Synonyms:C₃₂H₄₄O₅Si

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Chemical Property of C₃₂H₄₄O₅Si

Chemical Property:

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Technology Process of C₃₂H₄₄O₅Si

There total 12 articles about C₃₂H₄₄O₅Si 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: 78.0%

: 1292808-48-0
C₃₅H₄₈O₅Si

: 1292808-54-8
C₃₂H₄₄O₅Si

Guidance literature:: With trifluoroacetic acid; In tetrahydrofuran; water;
DOI:10.1016/j.bmcl.2011.02.021

Reference yield:

: 117621-80-4
C₁₀H₁₈O₃

: 1292808-54-8
C₃₂H₄₄O₅Si

Guidance literature:: Multi-step reaction with 4 steps

1: 1H-imidazole; iodine; triphenylphosphine / dichloromethane / 20 °C

2: acetonitrile / 48 h / 50 °C

3: n-butyllithium / tetrahydrofuran / -78 - 20 °C

4: trifluoroacetic acid / tetrahydrofuran; water

With 1H-imidazole; n-butyllithium; iodine; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; water; acetonitrile;
DOI:10.1016/j.bmcl.2011.02.021

Reference yield:

: 1292808-46-8
C₁₆H₃₂O₃Si

: 1292808-54-8
C₃₂H₄₄O₅Si

Guidance literature:: Multi-step reaction with 5 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 °C

2: 1H-imidazole; iodine; triphenylphosphine / dichloromethane / 20 °C

3: acetonitrile / 48 h / 50 °C

4: n-butyllithium / tetrahydrofuran / -78 - 20 °C

5: trifluoroacetic acid / tetrahydrofuran; water

With 1H-imidazole; n-butyllithium; tetrabutyl ammonium fluoride; iodine; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; water; acetonitrile;
DOI:10.1016/j.bmcl.2011.02.021