C₅₀H₅₀O₁₀

Base Information

Chemical Name:C₅₀H₅₀O₁₀
CAS No.:1585169-40-9
Molecular Formula:C₅₀H₅₀O₁₀
Molecular Weight:810.941
Hs Code.:

C<sub>50</sub>H<sub>50</sub>O<sub>10</sub>

Synonyms:C₅₀H₅₀O₁₀

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Chemical Property of C₅₀H₅₀O₁₀

Chemical Property:

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Technology Process of C₅₀H₅₀O₁₀

There total 6 articles about C₅₀H₅₀O₁₀ 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: 50.0%

: 1585169-39-6
C₅₀H₅₀O₉

: 1585169-40-9
C₅₀H₅₀O₁₀

Guidance literature:: With sodium chlorite; aminosulfonic acid; In water; acetone; at 0 ℃; for 0.333333h;
DOI:10.1021/ol500725e

Reference yield:

: 1585169-36-3
C₄₃H₄₅BrO₈

: 1585169-40-9
C₅₀H₅₀O₁₀

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium; isopropylmagnesium chloride / tetrahydrofuran; cyclohexane / 0.75 h / -78 - -20 °C

1.2: 0.5 h / -20 °C

2.1: sodium iodide; aluminum (III) chloride / acetonitrile / 1 h / 80 °C / Inert atmosphere

3.1: sodium hexamethyldisilazane / N,N-dimethyl-formamide; tetrahydrofuran / -78 - 20 °C / Inert atmosphere

3.2: 18 h / 20 °C / Inert atmosphere

4.1: sodium chlorite; aminosulfonic acid / acetone; water / 0.33 h / 0 °C

With aluminum (III) chloride; sodium chlorite; n-butyllithium; aminosulfonic acid; isopropylmagnesium chloride; sodium hexamethyldisilazane; sodium iodide; In tetrahydrofuran; cyclohexane; water; N,N-dimethyl-formamide; acetone; acetonitrile;
DOI:10.1021/ol500725e

Reference yield:

: 141196-74-9
1-trifluoroacetoxy-2,3,4,6-tetra-O-benzyl-α,β-D-glucopyranoside

: 1585169-40-9
C₅₀H₅₀O₁₀

Guidance literature:: Multi-step reaction with 5 steps

1.1: boron trifluoride diethyl etherate / dichloromethane / 0.5 h / 0 °C

2.1: n-butyllithium; N,N,N,N,-tetramethylethylenediamine

3.1: sodium iodide; aluminum (III) chloride / acetonitrile / 1 h / 80 °C / Inert atmosphere

4.1: sodium hexamethyldisilazane / N,N-dimethyl-formamide; tetrahydrofuran / -78 - 20 °C / Inert atmosphere

4.2: 18 h / 20 °C / Inert atmosphere

5.1: sodium chlorite; aminosulfonic acid / acetone; water / 0.33 h / 0 °C

With aluminum (III) chloride; sodium chlorite; n-butyllithium; N,N,N,N,-tetramethylethylenediamine; boron trifluoride diethyl etherate; aminosulfonic acid; sodium hexamethyldisilazane; sodium iodide; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; acetone; acetonitrile; 1.1: |Friedel-Crafts Alkylation;
DOI:10.1021/ol500725e