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C25H42O3

Base Information
  • Chemical Name:C25H42O3
  • CAS No.:1310801-74-1
  • Molecular Formula:C25H42O3
  • Molecular Weight:390.607
  • Hs Code.:
C<sub>25</sub>H<sub>42</sub>O<sub>3</sub>

Synonyms:C25H42O3

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Chemical Property of C25H42O3
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Technology Process of C25H42O3

There total 15 articles about C25H42O3 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 methanesulfonamide; AD-mix β; In water; tert-butyl alcohol; at 0 - 20 ℃; for 30h;
DOI:10.1016/j.tetlet.2011.03.089
Guidance literature:
Multi-step reaction with 5 steps
1: n-butyllithium; methyl-triphenylphosphonium iodide / tetrahydrofuran / 0 - 20 °C
2: toluene-4-sulfonic acid / methanol / 0.5 h / Reflux
3: dmap; triethylamine / dichloromethane / 4 h / 0 - 20 °C
4: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 10 h / Reflux
5: AD-mix β; methanesulfonamide / water; tert-butyl alcohol / 30 h / 0 - 20 °C
With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; dmap; n-butyllithium; methanesulfonamide; AD-mix β; methyl-triphenylphosphonium iodide; toluene-4-sulfonic acid; triethylamine; In tetrahydrofuran; methanol; dichloromethane; water; tert-butyl alcohol; 1: Wittig reaction / 4: Cross methathesis / 5: Sharpless asymmetric dihydroxylation;
DOI:10.1016/j.tetlet.2011.03.089
Guidance literature:
Multi-step reaction with 4 steps
1: toluene-4-sulfonic acid / methanol / 0.5 h / Reflux
2: dmap; triethylamine / dichloromethane / 4 h / 0 - 20 °C
3: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 10 h / Reflux
4: AD-mix β; methanesulfonamide / water; tert-butyl alcohol / 30 h / 0 - 20 °C
With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; dmap; methanesulfonamide; AD-mix β; toluene-4-sulfonic acid; triethylamine; In methanol; dichloromethane; water; tert-butyl alcohol; 3: Cross methathesis / 4: Sharpless asymmetric dihydroxylation;
DOI:10.1016/j.tetlet.2011.03.089
upstream raw materials:

C18H30O4

C18H28O4

C19H30O3

C17H26O2

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