4-[4-(2,5-bis-dodecyloxy-4-trimethylsilanylethynyl-phenylethynyl)-2,5-bis-dodecyloxy-phenylethynyl]-benzoic acid 2-trimethylsilanyl-ethyl ester

Base Information

Chemical Name:4-[4-(2,5-bis-dodecyloxy-4-trimethylsilanylethynyl-phenylethynyl)-2,5-bis-dodecyloxy-phenylethynyl]-benzoic acid 2-trimethylsilanyl-ethyl ester
CAS No.:860402-26-2
Molecular Formula:C₈₁H₁₃₀O₆Si₂
Molecular Weight:1256.09
Hs Code.:

4-[4-(2,5-bis-dodecyloxy-4-trimethylsilanylethynyl-phenylethynyl)-2,5-bis-dodecyloxy-phenylethynyl]-benzoic acid 2-trimethylsilanyl-ethyl ester

Synonyms:4-[4-(2,5-bis-dodecyloxy-4-trimethylsilanylethynyl-phenylethynyl)-2,5-bis-dodecyloxy-phenylethynyl]-benzoic acid 2-trimethylsilanyl-ethyl ester

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Chemical Property of 4-[4-(2,5-bis-dodecyloxy-4-trimethylsilanylethynyl-phenylethynyl)-2,5-bis-dodecyloxy-phenylethynyl]-benzoic acid 2-trimethylsilanyl-ethyl ester

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Technology Process of 4-[4-(2,5-bis-dodecyloxy-4-trimethylsilanylethynyl-phenylethynyl)-2,5-bis-dodecyloxy-phenylethynyl]-benzoic acid 2-trimethylsilanyl-ethyl ester

There total 7 articles about 4-[4-(2,5-bis-dodecyloxy-4-trimethylsilanylethynyl-phenylethynyl)-2,5-bis-dodecyloxy-phenylethynyl]-benzoic acid 2-trimethylsilanyl-ethyl ester 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: 84.0%

: 780755-58-0
4-(2,5-bis-dodecyloxy-4-ethynyl-phenylethynyl)-benzoic acid 2-trimethylsilanyl-ethyl ester

: 523978-90-7
1,4-bis(dodecyloxy)-2-[(trimethylsilyl)ethynyl]-5-iodobenzene

: 860402-26-2
4-[4-(2,5-bis-dodecyloxy-4-trimethylsilanylethynyl-phenylethynyl)-2,5-bis-dodecyloxy-phenylethynyl]-benzoic acid 2-trimethylsilanyl-ethyl ester

Guidance literature:: With copper(l) iodide; diisopropylamine; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; at 20 ℃; for 24h;
DOI:10.1081/SCC-200057287

Reference yield:

: 145483-66-5
1,4-bis(dodecyloxy)-2,5-diiodobenzene

: 860402-26-2
4-[4-(2,5-bis-dodecyloxy-4-trimethylsilanylethynyl-phenylethynyl)-2,5-bis-dodecyloxy-phenylethynyl]-benzoic acid 2-trimethylsilanyl-ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 47 percent / diisopropylamine; CuI / Pd(PPh₃)2Cl₂ / tetrahydrofuran / 24 h / 20 °C

2: 88 percent / diisopropylamine; CuI / Pd(PPh₃)2Cl₂ / tetrahydrofuran / 24 h / 20 °C

3: 99.1 percent / tetrabutylammonium fluoride / CH₂Cl₂ / 1 h / 20 °C

4: 84 percent / diisopropylamine; CuI / Pd(PPh₃)2Cl₂ / tetrahydrofuran / 24 h / 20 °C

With copper(l) iodide; tetrabutyl ammonium fluoride; diisopropylamine; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; dichloromethane;
DOI:10.1081/SCC-200057287

Reference yield:

: 860402-21-7
4-trimethylsilanylethynyl-benzoic acid 2-trimethylsilanyl-ethyl ester

: 860402-26-2
4-[4-(2,5-bis-dodecyloxy-4-trimethylsilanylethynyl-phenylethynyl)-2,5-bis-dodecyloxy-phenylethynyl]-benzoic acid 2-trimethylsilanyl-ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 89 percent / tetrabutylammonium fluoride / CH₂Cl₂ / 1 h / 20 °C

2: 88 percent / diisopropylamine; CuI / Pd(PPh₃)2Cl₂ / tetrahydrofuran / 24 h / 20 °C

3: 99.1 percent / tetrabutylammonium fluoride / CH₂Cl₂ / 1 h / 20 °C

4: 84 percent / diisopropylamine; CuI / Pd(PPh₃)2Cl₂ / tetrahydrofuran / 24 h / 20 °C

With copper(l) iodide; tetrabutyl ammonium fluoride; diisopropylamine; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; dichloromethane;
DOI:10.1081/SCC-200057287