C₂₆H₃₅ClO₇

Base Information

Chemical Name:C₂₆H₃₅ClO₇
CAS No.:1621624-05-2
Molecular Formula:C₂₆H₃₅ClO₇
Molecular Weight:495.013
Hs Code.:

C<sub>26</sub>H<sub>35</sub>ClO<sub>7</sub>

Synonyms:C₂₆H₃₅ClO₇

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Chemical Property of C₂₆H₃₅ClO₇

Chemical Property:

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Technology Process of C₂₆H₃₅ClO₇

There total 14 articles about C₂₆H₃₅ClO₇ 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: 49.0%

: C₃₃H₄₂O₆

: 1621624-05-2
C₂₆H₃₅ClO₇

Guidance literature:: With N-chloro-succinimide; osmium(VIII) oxide; water; In acetone; tert-butyl alcohol; for 8h;

Reference yield:

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

: 1621624-05-2
C₂₆H₃₅ClO₇

Guidance literature:: Multi-step reaction with 10 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 / 0.75 h / 20 °C

10.1: N-chloro-succinimide; osmium(VIII) oxide; water / tert-butyl alcohol; acetone / 8 h

With N-chloro-succinimide; 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; acetone; toluene; tert-butyl alcohol;

Reference yield:

: 1333067-66-5
C₂₄H₂₉NO₆

: 1621624-05-2
C₂₆H₃₅ClO₇

Guidance literature:: Multi-step reaction with 9 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 / 0.75 h / 20 °C

9.1: N-chloro-succinimide; osmium(VIII) oxide; water / tert-butyl alcohol; acetone / 8 h

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