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1,4-bis[ethoxy(thiocarbonyl)thiomethyl]-2-(2'-ethylhexyloxy)-5-(phenylethynyl)benzenen

Base Information
  • Chemical Name:1,4-bis[ethoxy(thiocarbonyl)thiomethyl]-2-(2'-ethylhexyloxy)-5-(phenylethynyl)benzenen
  • CAS No.:263708-07-2
  • Molecular Formula:C30H38O3S4
  • Molecular Weight:574.894
  • Hs Code.:
1,4-bis[ethoxy(thiocarbonyl)thiomethyl]-2-(2'-ethylhexyloxy)-5-(phenylethynyl)benzenen

Synonyms:1,4-bis[ethoxy(thiocarbonyl)thiomethyl]-2-(2'-ethylhexyloxy)-5-(phenylethynyl)benzenen

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Chemical Property of 1,4-bis[ethoxy(thiocarbonyl)thiomethyl]-2-(2'-ethylhexyloxy)-5-(phenylethynyl)benzenen
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Technology Process of 1,4-bis[ethoxy(thiocarbonyl)thiomethyl]-2-(2'-ethylhexyloxy)-5-(phenylethynyl)benzenen

There total 7 articles about 1,4-bis[ethoxy(thiocarbonyl)thiomethyl]-2-(2'-ethylhexyloxy)-5-(phenylethynyl)benzenen 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:
Guidance literature:
Multi-step reaction with 4 steps
1: 93 percent / pyridine / 9.5 h / Heating
2: 96 percent / aq. NaOH / CH2Cl2; methanol / 5 h / 20 °C
3: 49 percent / phosphorus tribromide / diethyl ether / 1 h / 20 °C
4: 96 percent / tetra(n-butyl)ammonium bromide / CH2Cl2 / 18 h / 20 °C
With pyridine; sodium hydroxide; tetrabutylammomium bromide; phosphorus tribromide; In methanol; diethyl ether; dichloromethane; 1: Substitution / 2: Hydrolysis / 3: Bromination / 4: xanthation;
DOI:10.1039/a904274a
Guidance literature:
Multi-step reaction with 6 steps
1: 97 percent / pyridine / 4.5 h / Heating
2: 97 percent / iodine; silver acetate / CHCl3 / 4.5 h / 20 °C
3: 93 percent / pyridine / 9.5 h / Heating
4: 96 percent / aq. NaOH / CH2Cl2; methanol / 5 h / 20 °C
5: 49 percent / phosphorus tribromide / diethyl ether / 1 h / 20 °C
6: 96 percent / tetra(n-butyl)ammonium bromide / CH2Cl2 / 18 h / 20 °C
With pyridine; sodium hydroxide; tetrabutylammomium bromide; iodine; silver(I) acetate; phosphorus tribromide; In methanol; diethyl ether; dichloromethane; chloroform; 1: Acetylation / 2: Iodination / 3: Substitution / 4: Hydrolysis / 5: Bromination / 6: xanthation;
DOI:10.1039/a904274a
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