C₄₁H₅₈O₁₉

Base Information

Chemical Name:C₄₁H₅₈O₁₉
CAS No.:1351377-49-5
Molecular Formula:C₄₁H₅₈O₁₉
Molecular Weight:854.9
Hs Code.:

C<sub>41</sub>H<sub>58</sub>O<sub>19</sub>

Synonyms:C₄₁H₅₈O₁₉

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Chemical Property of C₄₁H₅₈O₁₉

Chemical Property:

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Technology Process of C₄₁H₅₈O₁₉

There total 11 articles about C₄₁H₅₈O₁₉ 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:

: 1350963-43-7
C₁₈H₂₆O₇S

: 1351377-49-5
C₄₁H₅₈O₁₉

Guidance literature:: Multi-step reaction with 10 steps

1.1: tetrabutylammomium bromide; sodium hydroxide / water / 40 h / 70 °C

2.1: water; acetic acid / 12 h / 25 °C

3.1: triethylamine / dichloromethane

4.1: sodium iodide / 1,2-dimethoxyethane

5.1: dimethylsulfide borane complex / tetrahydrofuran / 20 h / 0 °C

5.2: 3 h / 25 °C

6.1: sodium hydride / tetrahydrofuran / 12 h / 0 - 25 °C

7.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 15 h / 25 °C

8.1: tetrabutylammomium bromide; sodium hydroxide / water / 30 h / 60 °C

9.1: acetic acid / 7 h / Reflux

10.1: pyridine; dmap / 12 h / 0 - 25 °C

With pyridine; dmap; dimethylsulfide borane complex; palladium 10% on activated carbon; tetrabutylammomium bromide; water; hydrogen; sodium hydride; acetic acid; triethylamine; sodium iodide; sodium hydroxide; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; water; ethyl acetate;
DOI:10.1016/j.tetlet.2011.09.139

Reference yield:

: 314061-35-3
2-((3aR,5R,6R,6aR)-6-Benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanol

: 1351377-49-5
C₄₁H₅₈O₁₉

Guidance literature:: Multi-step reaction with 11 steps

1.1: triethylamine / dichloromethane / 4 h / 0 - 20 °C

2.1: tetrabutylammomium bromide; sodium hydroxide / water / 40 h / 70 °C

3.1: water; acetic acid / 12 h / 25 °C

4.1: triethylamine / dichloromethane

5.1: sodium iodide / 1,2-dimethoxyethane

6.1: dimethylsulfide borane complex / tetrahydrofuran / 20 h / 0 °C

6.2: 3 h / 25 °C

7.1: sodium hydride / tetrahydrofuran / 12 h / 0 - 25 °C

8.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 15 h / 25 °C

9.1: tetrabutylammomium bromide; sodium hydroxide / water / 30 h / 60 °C

10.1: acetic acid / 7 h / Reflux

11.1: pyridine; dmap / 12 h / 0 - 25 °C

With pyridine; dmap; dimethylsulfide borane complex; palladium 10% on activated carbon; tetrabutylammomium bromide; water; hydrogen; sodium hydride; acetic acid; triethylamine; sodium iodide; sodium hydroxide; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; water; ethyl acetate;
DOI:10.1016/j.tetlet.2011.09.139

Reference yield:

: 1350963-47-1
C₂₇H₄₀O₉

: 1351377-49-5
C₄₁H₅₈O₁₉

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydride / tetrahydrofuran / 12 h / 0 - 25 °C

2: palladium 10% on activated carbon; hydrogen / ethyl acetate / 15 h / 25 °C

3: tetrabutylammomium bromide; sodium hydroxide / water / 30 h / 60 °C

4: acetic acid / 7 h / Reflux

5: pyridine; dmap / 12 h / 0 - 25 °C

With pyridine; dmap; palladium 10% on activated carbon; tetrabutylammomium bromide; hydrogen; sodium hydride; acetic acid; sodium hydroxide; In tetrahydrofuran; water; ethyl acetate;
DOI:10.1016/j.tetlet.2011.09.139