C₂₆H₂₈O₁₀

Base Information

Chemical Name:C₂₆H₂₈O₁₀
CAS No.:1262887-42-2
Molecular Formula:C₂₆H₂₈O₁₀
Molecular Weight:500.502
Hs Code.:

C<sub>26</sub>H<sub>28</sub>O<sub>10</sub>

Synonyms:C₂₆H₂₈O₁₀

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₂₆H₂₈O₁₀

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Technology Process of C₂₆H₂₈O₁₀

There total 16 articles about C₂₆H₂₈O₁₀ 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: 91.0%

: 1262887-41-1
C₄₂H₄₆O₁₀Si

: 1262887-42-2
C₂₆H₂₈O₁₀

Guidance literature:: With tetrabutyl ammonium fluoride; acetic acid; In tetrahydrofuran; at 0 - 20 ℃; for 6h; Inert atmosphere; Industry scale;

Reference yield:

: 40608-06-8
levulinic anhydride

: 1262887-42-2
C₂₆H₂₈O₁₀

Guidance literature:: Multi-step reaction with 5 steps

1: dmap; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 16 h / 20 °C / Inert atmosphere; Industry scale

2: trifluoroacetic acid / 4 h / 20 °C / Industry scale

3: 1H-imidazole / dichloromethane / 3 h / 20 °C / Inert atmosphere; Industry scale

4: pyridine / dichloromethane / 3 h / -20 - 20 °C / Inert atmosphere; Industry scale

5: tetrabutyl ammonium fluoride; acetic acid / tetrahydrofuran / 6 h / 0 - 20 °C / Inert atmosphere; Industry scale

With pyridine; 1H-imidazole; dmap; tetrabutyl ammonium fluoride; acetic acid; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;

Reference yield:

: C₁₇H₂₂O₇

: 1262887-42-2
C₂₆H₂₈O₁₀

Guidance literature:: Multi-step reaction with 5 steps

1: N-ethyl-N,N-diisopropylamine / dmap / tetrahydrofuran / 10 - 20 °C / Inert atmosphere

2: trifluoroacetic acid / 5 °C

3: 1H-imidazole / dichloromethane / 3 h / -20 - 20 °C

4: pyridine / dichloromethane / 3 h / -20 - 20 °C / Inert atmosphere

5: 1H-imidazole; tetrabutyl ammonium fluoride; acetic acid / tetrahydrofuran / 6 h / 0 - 20 °C / Inert atmosphere

With pyridine; 1H-imidazole; tetrabutyl ammonium fluoride; acetic acid; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; dmap; In tetrahydrofuran; dichloromethane;