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C26H34O4Si

Base Information
  • Chemical Name:C26H34O4Si
  • CAS No.:1209497-06-2
  • Molecular Formula:C26H34O4Si
  • Molecular Weight:438.639
  • Hs Code.:
C<sub>26</sub>H<sub>34</sub>O<sub>4</sub>Si

Synonyms:C26H34O4Si

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Chemical Property of C26H34O4Si
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Technology Process of C26H34O4Si

There total 10 articles about C26H34O4Si 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:
Guidance literature:
With palladium 10% on activated carbon; hydrogen; In ethyl acetate; for 20h; under 760.051 Torr;
DOI:10.1002/ejoc.201100062
Guidance literature:
Multi-step reaction with 9 steps
1.1: Umicore M2 / dichloromethane / 70 h / 20 °C / Inert atmosphere; Darkness
2.1: dipyridinium dichromate / dichloromethane / 72 h / 20 °C / Molecular sieve
3.1: tetrahydrofuran / 0.5 h / -78 °C
3.2: 2 h / 20 °C
4.1: bromine / dichloromethane / 2 h / 20 °C
4.2: 0.33 h / 20 °C
4.3: 16 h / -78 - -30 °C
5.1: potassium carbonate / methanol / 12 h / 20 °C
6.1: N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid / 1,2-dichloro-ethane / -30 - 20 °C / Reflux
7.1: sodium methylate / methanol / 0.25 h / -30 - 0 °C
8.1: toluene-4-sulfonic acid; 2,2-dimethoxy-propane / 13 h / 20 °C
9.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 20 h / 760.05 Torr
With dipyridinium dichromate; palladium 10% on activated carbon; hydrogen; bromine; sodium methylate; potassium carbonate; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; 2,2-dimethoxy-propane; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; 1,2-dichloro-ethane;
DOI:10.1002/ejoc.201100062
Guidance literature:
Multi-step reaction with 7 steps
1.1: tetrahydrofuran / 0.5 h / -78 °C
1.2: 2 h / 20 °C
2.1: bromine / dichloromethane / 2 h / 20 °C
2.2: 0.33 h / 20 °C
2.3: 16 h / -78 - -30 °C
3.1: potassium carbonate / methanol / 12 h / 20 °C
4.1: N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid / 1,2-dichloro-ethane / -30 - 20 °C / Reflux
5.1: sodium methylate / methanol / 0.25 h / -30 - 0 °C
6.1: toluene-4-sulfonic acid; 2,2-dimethoxy-propane / 13 h / 20 °C
7.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 20 h / 760.05 Torr
With palladium 10% on activated carbon; hydrogen; bromine; sodium methylate; potassium carbonate; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; 2,2-dimethoxy-propane; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; 1,2-dichloro-ethane;
DOI:10.1002/ejoc.201100062
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