C₄₆H₅₇N₈O₁₄Si⁽¹⁺⁾*Cl^(1-)

Base Information

Chemical Name:C₄₆H₅₇N₈O₁₄Si⁽¹⁺⁾*Cl^(1-)
CAS No.:1352660-53-7
Molecular Formula:C₄₆H₅₇N₈O₁₄Si*Cl
Molecular Weight:1009.54
Hs Code.:

C<sub>46</sub>H<sub>57</sub>N<sub>8</sub>O<sub>14</sub>Si<sup>(1+)</sup>*Cl<sup>(1-)</sup>

Synonyms:C₄₆H₅₇N₈O₁₄Si⁽¹⁺⁾*Cl^(1-)

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Chemical Property of C₄₆H₅₇N₈O₁₄Si⁽¹⁺⁾*Cl^(1-)

Chemical Property:

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Technology Process of C₄₆H₅₇N₈O₁₄Si⁽¹⁺⁾*Cl^(1-)

There total 10 articles about C₄₆H₅₇N₈O₁₄Si⁽¹⁺⁾*Cl^(1-) 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:

: 1352660-50-4
C₄₅H₅₄N₈O₁₄Si

: 74-88-4
methyl iodide

: 1352660-53-7
C₄₆H₅₇N₈O₁₄Si⁽¹⁺⁾*Cl^(1-)

Guidance literature:: C₄₅H₅₄N₈O₁₄Si; methyl iodide; In tetrahydrofuran; at 0 - 20 ℃; for 72h;

With sodium chloride; In water;

Reference yield:

: C₃₄H₅₇NO₈Si₂

: 1352660-53-7
C₄₆H₅₇N₈O₁₄Si⁽¹⁺⁾*Cl^(1-)

Guidance literature:: Multi-step reaction with 7 steps

1: hydrogen; formic acid / ethyl acetate / 2068.65 - 2585.81 Torr / Catalyst

2: hydrogenchloride / acetonitrile

3: 1H-imidazole / Solvent

4: Alkaline conditions; Solvent

5: triethyl phosphite / Solvent; Reflux

6: 2,6-dimethylpyridine / triethyl phosphite; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex / N,N-dimethyl-formamide / 48 h / 20 °C

7: tetrahydrofuran / 72 h / 0 - 20 °C

With 1H-imidazole; 2,6-dimethylpyridine; hydrogenchloride; formic acid; hydrogen; triethyl phosphite; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; triethyl phosphite; In tetrahydrofuran; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: C₂₈H₄₃NO₈Si

: 1352660-53-7
C₄₆H₅₇N₈O₁₄Si⁽¹⁺⁾*Cl^(1-)

Guidance literature:: Multi-step reaction with 8 steps

1: Solvent; Heating; Alkaline conditions

2: hydrogen; formic acid / ethyl acetate / 2068.65 - 2585.81 Torr / Catalyst

3: hydrogenchloride / acetonitrile

4: 1H-imidazole / Solvent

5: Alkaline conditions; Solvent

6: triethyl phosphite / Solvent; Reflux

7: 2,6-dimethylpyridine / triethyl phosphite; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex / N,N-dimethyl-formamide / 48 h / 20 °C

8: tetrahydrofuran / 72 h / 0 - 20 °C

With 1H-imidazole; 2,6-dimethylpyridine; hydrogenchloride; formic acid; hydrogen; triethyl phosphite; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; triethyl phosphite; In tetrahydrofuran; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;