C₂₆H₃₄O₅

Base Information

Chemical Name:C₂₆H₃₄O₅
CAS No.:1209386-63-9
Molecular Formula:C₂₆H₃₄O₅
Molecular Weight:426.553
Hs Code.:

C<sub>26</sub>H<sub>34</sub>O<sub>5</sub>

Synonyms:C₂₆H₃₄O₅

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Chemical Property of C₂₆H₃₄O₅

Chemical Property:

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Technology Process of C₂₆H₃₄O₅

There total 5 articles about C₂₆H₃₄O₅ 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: 99.0%

: 1209386-07-1
C₂₆H₃₆O₅

: 1209386-63-9
C₂₆H₃₄O₅

Guidance literature:: With sulfur trioxide pyridine complex; dimethyl sulfoxide; triethylamine; In dichloromethane; at 0 ℃; for 1.5h; Inert atmosphere;
DOI:10.1021/jo400260m

Reference yield:

: C₁₉H₂₈O₄

: 1209386-63-9
C₂₆H₃₄O₅

Guidance literature:: Multi-step reaction with 4 steps

1: trifluorormethanesulfonic acid / dichloromethane; cyclohexane / 0.5 h / 20 °C / Inert atmosphere

2: diisobutylaluminium hydride / dichloromethane; hexane / 0.08 h / -78 °C / Inert atmosphere

3: L-(+)-diisopropyl tartrate; titanium(IV) isopropylate; tert.-butylhydroperoxide / dichloromethane; decane / -20 °C / Inert atmosphere; Molecular sieve

4: dimethyl sulfoxide; sulfur trioxide pyridine complex; triethylamine / dichloromethane / 1.5 h / 0 °C / Inert atmosphere

With titanium(IV) isopropylate; tert.-butylhydroperoxide; L-(+)-diisopropyl tartrate; trifluorormethanesulfonic acid; sulfur trioxide pyridine complex; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; In decane; hexane; dichloromethane; cyclohexane; 3: |Sharpless Asymmetric Epoxidation / 4: |Parikh-Doering Oxidation;
DOI:10.1021/jo400260m

Reference yield:

: C₁₈H₂₄O₄

: 1209386-63-9
C₂₆H₃₄O₅

Guidance literature:: Multi-step reaction with 5 steps

1: water; trimethylaluminum / dichloromethane; hexane / -40 - 0 °C / Inert atmosphere

2: trifluorormethanesulfonic acid / dichloromethane; cyclohexane / 0.5 h / 20 °C / Inert atmosphere

3: diisobutylaluminium hydride / dichloromethane; hexane / 0.08 h / -78 °C / Inert atmosphere

4: L-(+)-diisopropyl tartrate; titanium(IV) isopropylate; tert.-butylhydroperoxide / dichloromethane; decane / -20 °C / Inert atmosphere; Molecular sieve

5: dimethyl sulfoxide; sulfur trioxide pyridine complex; triethylamine / dichloromethane / 1.5 h / 0 °C / Inert atmosphere

With titanium(IV) isopropylate; tert.-butylhydroperoxide; L-(+)-diisopropyl tartrate; trifluorormethanesulfonic acid; water; trimethylaluminum; sulfur trioxide pyridine complex; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; In decane; hexane; dichloromethane; cyclohexane; 4: |Sharpless Asymmetric Epoxidation / 5: |Parikh-Doering Oxidation;
DOI:10.1021/jo400260m