{2-(2-ethoxy-ethoxy)-4-[2-(2-ethoxy-ethoxy)-4-iodo-phenylethynyl]-phenylethynyl}-trimethyl-silane

Base Information

Chemical Name:{2-(2-ethoxy-ethoxy)-4-[2-(2-ethoxy-ethoxy)-4-iodo-phenylethynyl]-phenylethynyl}-trimethyl-silane
CAS No.:220630-13-7
Molecular Formula:C₂₇H₃₃IO₄Si
Molecular Weight:576.547
Hs Code.:

Synonyms:{2-(2-ethoxy-ethoxy)-4-[2-(2-ethoxy-ethoxy)-4-iodo-phenylethynyl]-phenylethynyl}-trimethyl-silane

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Chemical Property of {2-(2-ethoxy-ethoxy)-4-[2-(2-ethoxy-ethoxy)-4-iodo-phenylethynyl]-phenylethynyl}-trimethyl-silane

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Technology Process of {2-(2-ethoxy-ethoxy)-4-[2-(2-ethoxy-ethoxy)-4-iodo-phenylethynyl]-phenylethynyl}-trimethyl-silane

There total 8 articles about {2-(2-ethoxy-ethoxy)-4-[2-(2-ethoxy-ethoxy)-4-iodo-phenylethynyl]-phenylethynyl}-trimethyl-silane 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: 97.0%

: 220630-16-0
C₃₁H₄₃N₃O₄Si

: 220630-13-7
{2-(2-ethoxy-ethoxy)-4-[2-(2-ethoxy-ethoxy)-4-iodo-phenylethynyl]-phenylethynyl}-trimethyl-silane

Guidance literature:: With methyl iodide; at 130 ℃; for 17h;
DOI:10.1002/(SICI)1521-3773(19981204)37:22<3154::AID-ANIE3154>3.0.CO;2-W

Reference yield:

: 40547-58-8
N-(4-acetyl-3-hydroxyphenyl)acetamide

: 220630-13-7
{2-(2-ethoxy-ethoxy)-4-[2-(2-ethoxy-ethoxy)-4-iodo-phenylethynyl]-phenylethynyl}-trimethyl-silane

Guidance literature:: Multi-step reaction with 7 steps

1: 75 percent / K₂CO₃ / dimethylformamide / 5 h / 20 °C

2: 81 percent / HCl, H₂O / 100 °C

3: 1.) NaNO₂ / 1.) H₂O, 0 deg C, 15 min, 2.) H₂O, 0 deg C, 15 min

5: 78 percent / MeI / 17 h / 130 °C

6: 97 percent / CuI, pyrrolidine / 2(dba)3> / 20 °C

7: 97 percent / MeI / 17 h / 130 °C

With pyrrolidine; hydrogenchloride; copper(l) iodide; water; potassium carbonate; sodium nitrite; methyl iodide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In N,N-dimethyl-formamide;
DOI:10.1002/(SICI)1521-3773(19981204)37:22<3154::AID-ANIE3154>3.0.CO;2-W

Reference yield:

: 95493-65-5
(5-Acetamino-2-acetyl-phenyl)-(2-ethoxy-ethyl)-ether

: 220630-13-7
{2-(2-ethoxy-ethoxy)-4-[2-(2-ethoxy-ethoxy)-4-iodo-phenylethynyl]-phenylethynyl}-trimethyl-silane

Guidance literature:: Multi-step reaction with 6 steps

1: 81 percent / HCl, H₂O / 100 °C

2: 1.) NaNO₂ / 1.) H₂O, 0 deg C, 15 min, 2.) H₂O, 0 deg C, 15 min

4: 78 percent / MeI / 17 h / 130 °C

5: 97 percent / CuI, pyrrolidine / 2(dba)3> / 20 °C

6: 97 percent / MeI / 17 h / 130 °C

With pyrrolidine; hydrogenchloride; copper(l) iodide; water; sodium nitrite; methyl iodide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾;
DOI:10.1002/(SICI)1521-3773(19981204)37:22<3154::AID-ANIE3154>3.0.CO;2-W