C₃₆H₃₆F₆O₁₀

Base Information

Chemical Name:C₃₆H₃₆F₆O₁₀
CAS No.:1374332-23-6
Molecular Formula:C₃₆H₃₆F₆O₁₀
Molecular Weight:742.666
Hs Code.:

C<sub>36</sub>H<sub>36</sub>F<sub>6</sub>O<sub>10</sub>

Synonyms:

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Chemical Property of C₃₆H₃₆F₆O₁₀

Chemical Property:

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Technology Process of C₃₆H₃₆F₆O₁₀

There total 5 articles about C₃₆H₃₆F₆O₁₀ 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:

: 1374332-17-8
(2E,4E)-methyl 7-((4-methoxybenzyl)oxy)hepta-2,4-dienoate

: 1374332-23-6
C₃₆H₃₆F₆O₁₀

Guidance literature:: Multi-step reaction with 2 steps

1: K₂Os(OH)2; methanesulfonamide; potassium carbonate; hydroquinidein 1,4-phthalazinediyl diether; potassium hexacyanoferrate(III) / dichloromethane; water; tert-butyl alcohol / 24 h / 0 °C / Inert atmosphere

2: pyridine / 3.25 h / 0 - 20 °C / Inert atmosphere

With methanesulfonamide; K₂Os(OH)2; potassium carbonate; hydroquinidein 1,4-phthalazinediyl diether; potassium hexacyanoferrate(III); In pyridine; dichloromethane; water; tert-butyl alcohol; 1: Mosher ester derivatization / 2: Mosher ester derivatization;
DOI:10.1021/ja302260d

Reference yield:

: 142860-83-1
1-(4-methoxybenzyloxy)-3-butene

: 1374332-23-6
C₃₆H₃₆F₆O₁₀

Guidance literature:: Multi-step reaction with 4 steps

1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 16 h / Inert atmosphere; Reflux

2: 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride / water; acetonitrile / 0.83 h / 0 - 20 °C / Inert atmosphere

3: K₂Os(OH)2; methanesulfonamide; potassium carbonate; hydroquinidein 1,4-phthalazinediyl diether; potassium hexacyanoferrate(III) / dichloromethane; water; tert-butyl alcohol / 24 h / 0 °C / Inert atmosphere

4: pyridine / 3.25 h / 0 - 20 °C / Inert atmosphere

With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; methanesulfonamide; K₂Os(OH)2; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; hydroquinidein 1,4-phthalazinediyl diether; lithium chloride; potassium hexacyanoferrate(III); In pyridine; dichloromethane; water; acetonitrile; tert-butyl alcohol; 2: Horner-Wadsworth-Emmons olefination / 3: Mosher ester derivatization / 4: Mosher ester derivatization;
DOI:10.1021/ja302260d

Reference yield:

: 824-94-2
p-methoxybenzyl chloride

: 1374332-23-6
C₃₆H₃₆F₆O₁₀

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydride / N,N-dimethyl-formamide / Inert atmosphere

2: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 16 h / Inert atmosphere; Reflux

3: 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride / water; acetonitrile / 0.83 h / 0 - 20 °C / Inert atmosphere

4: K₂Os(OH)2; methanesulfonamide; potassium carbonate; hydroquinidein 1,4-phthalazinediyl diether; potassium hexacyanoferrate(III) / dichloromethane; water; tert-butyl alcohol / 24 h / 0 °C / Inert atmosphere

5: pyridine / 3.25 h / 0 - 20 °C / Inert atmosphere

With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; methanesulfonamide; K₂Os(OH)2; sodium hydride; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; hydroquinidein 1,4-phthalazinediyl diether; lithium chloride; potassium hexacyanoferrate(III); In pyridine; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol; 3: Horner-Wadsworth-Emmons olefination / 4: Mosher ester derivatization / 5: Mosher ester derivatization;
DOI:10.1021/ja302260d