C₆₃H₁₀₂O₂₈

Base Information

Chemical Name:C₆₃H₁₀₂O₂₈
CAS No.:1017968-13-6
Molecular Formula:C₆₃H₁₀₂O₂₈
Molecular Weight:1307.49
Hs Code.:

C<sub>63</sub>H<sub>102</sub>O<sub>28</sub>

Synonyms:C₆₃H₁₀₂O₂₈

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Chemical Property of C₆₃H₁₀₂O₂₈

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Technology Process of C₆₃H₁₀₂O₂₈

There total 6 articles about C₆₃H₁₀₂O₂₈ 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: 88.0%

: 1017967-79-1
C₆₄H₁₀₄O₂₈

: 1017968-13-6
C₆₃H₁₀₂O₂₈

Guidance literature:: With sodium hydroxide; In tetrahydrofuran; water; for 2h; Inert atmosphere; Reflux;
DOI:10.1039/b9nj00305c

Reference yield:

: 62921-74-8,518012-62-9,58320-73-3
2-(2-(2-methoxyethoxy)ethoxy)ethyl p-toluenesulfonate

: 1017968-13-6
C₆₃H₁₀₂O₂₈

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate; potassium iodide / N,N-dimethyl-formamide / 12 h / 80 °C

2: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 60 °C

3: thionyl chloride / dichloromethane / 3 h / 20 °C

4: potassium carbonate; potassium iodide / N,N-dimethyl-formamide / 12 h / 80 °C

5: potassium hydroxide / tetrahydrofuran; water; methanol / 4 h / 50 °C

With lithium aluminium tetrahydride; thionyl chloride; potassium carbonate; potassium iodide; potassium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; 1: |Williamson Ether Synthesis / 4: |Williamson Ether Synthesis;
DOI:10.1021/acs.chemmater.7b02928

Reference yield:

: 852628-92-3
methyl 3,4,5-tris(2-(2-(2-methoxyethoxy)ethoxy)-ethoxy)benzoate

: 1017968-13-6
C₆₃H₁₀₂O₂₈

Guidance literature:: Multi-step reaction with 4 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 60 °C

2: thionyl chloride / dichloromethane / 3 h / 20 °C

3: potassium carbonate; potassium iodide / N,N-dimethyl-formamide / 12 h / 80 °C

4: potassium hydroxide / tetrahydrofuran; water; methanol / 4 h / 50 °C

With lithium aluminium tetrahydride; thionyl chloride; potassium carbonate; potassium iodide; potassium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; 3: |Williamson Ether Synthesis;
DOI:10.1021/acs.chemmater.7b02928