C₂₆H₃₈O₈

Base Information

Chemical Name:C₂₆H₃₈O₈
CAS No.:1621623-82-2
Molecular Formula:C₂₆H₃₈O₈
Molecular Weight:478.583
Hs Code.:

C<sub>26</sub>H<sub>38</sub>O<sub>8</sub>

Synonyms:

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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 C₂₆H₃₈O₈

Chemical Property:

Purity/Quality:

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Technology Process of C₂₆H₃₈O₈

There total 12 articles about C₂₆H₃₈O₈ 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:

: 1333067-50-7
C₂₂H₂₃NO₅

: 1621623-82-2
C₂₆H₃₈O₈

Guidance literature:: Multi-step reaction with 7 steps

1.1: n-butyllithium / hexane; diethyl ether / 1 h / -78 °C

1.2: 0.17 h / -78 - 0 °C

1.3: 11 h / 10 °C

2.1: trifluoroacetic acid; water / acetic acid / 14 h / 20 °C

3.1: methyllithium / tetrahydrofuran / 0.5 h / -78 °C

3.2: 1 h / -78 °C

3.3: 2 h / -78 - 20 °C

4.1: triethylamine; methanesulfonyl chloride / diethyl ether / 1.33 h / 0 - 20 °C

4.2: 1 h / -35 - 20 °C

5.1: trifluoroacetic acid; water / acetic acid / 1 h / 20 °C

6.1: triethylamine; 2,4,6-trichlorobenzoyl chloride / toluene / 6 h / 20 °C

6.2: 2 h / 80 °C

7.1: osmium(VIII) oxide; water / tert-butyl alcohol / 4 h / 20 °C

With osmium(VIII) oxide; n-butyllithium; 2,4,6-trichlorobenzoyl chloride; water; methyllithium; methanesulfonyl chloride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; diethyl ether; hexane; acetic acid; toluene; tert-butyl alcohol;

Reference yield:

: 1352810-66-2
(R)-4-benzyl-3-((2R,3R)-3-hydroxy-4,4-dimethoxy-2-methylbutanoyl)-oxazolidin-2-one

: 1621623-82-2
C₂₆H₃₈O₈

Guidance literature:: Multi-step reaction with 9 steps

1.1: silver(l) oxide / dichloromethane / 48 h / 20 °C / Molecular sieve; Inert atmosphere; Darkness

2.1: trifluoroacetic acid; water / acetic acid / 3.5 h / 20 °C

3.1: n-butyllithium / hexane; diethyl ether / 1 h / -78 °C

3.2: 0.17 h / -78 - 0 °C

3.3: 11 h / 10 °C

4.1: trifluoroacetic acid; water / acetic acid / 14 h / 20 °C

5.1: methyllithium / tetrahydrofuran / 0.5 h / -78 °C

5.2: 1 h / -78 °C

5.3: 2 h / -78 - 20 °C

6.1: triethylamine; methanesulfonyl chloride / diethyl ether / 1.33 h / 0 - 20 °C

6.2: 1 h / -35 - 20 °C

7.1: trifluoroacetic acid; water / acetic acid / 1 h / 20 °C

8.1: triethylamine; 2,4,6-trichlorobenzoyl chloride / toluene / 6 h / 20 °C

8.2: 2 h / 80 °C

9.1: osmium(VIII) oxide; water / tert-butyl alcohol / 4 h / 20 °C

With osmium(VIII) oxide; n-butyllithium; 2,4,6-trichlorobenzoyl chloride; water; methyllithium; methanesulfonyl chloride; triethylamine; trifluoroacetic acid; silver(l) oxide; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; acetic acid; toluene; tert-butyl alcohol;

Reference yield:

: 1333067-66-5
C₂₄H₂₉NO₆

: 1621623-82-2
C₂₆H₃₈O₈

Guidance literature:: Multi-step reaction with 8 steps

1.1: trifluoroacetic acid; water / acetic acid / 3.5 h / 20 °C

2.1: n-butyllithium / hexane; diethyl ether / 1 h / -78 °C

2.2: 0.17 h / -78 - 0 °C

2.3: 11 h / 10 °C

3.1: trifluoroacetic acid; water / acetic acid / 14 h / 20 °C

4.1: methyllithium / tetrahydrofuran / 0.5 h / -78 °C

4.2: 1 h / -78 °C

4.3: 2 h / -78 - 20 °C

5.1: triethylamine; methanesulfonyl chloride / diethyl ether / 1.33 h / 0 - 20 °C

5.2: 1 h / -35 - 20 °C

6.1: trifluoroacetic acid; water / acetic acid / 1 h / 20 °C

7.1: triethylamine; 2,4,6-trichlorobenzoyl chloride / toluene / 6 h / 20 °C

7.2: 2 h / 80 °C

8.1: osmium(VIII) oxide; water / tert-butyl alcohol / 4 h / 20 °C

With osmium(VIII) oxide; n-butyllithium; 2,4,6-trichlorobenzoyl chloride; water; methyllithium; methanesulfonyl chloride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; diethyl ether; hexane; acetic acid; toluene; tert-butyl alcohol;