4-(2-(5-(2-(4-(3,6-di-tert-butyl-9H-carbazolyl)phenyl)ethynyl)-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde

Base Information

Chemical Name:4-(2-(5-(2-(4-(3,6-di-tert-butyl-9H-carbazolyl)phenyl)ethynyl)-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde
CAS No.:1374843-11-4
Molecular Formula:C₄₅H₃₇NOS₂
Molecular Weight:671.927
Hs Code.:

Synonyms:4-(2-(5-(2-(4-(3,6-di-tert-butyl-9H-carbazolyl)phenyl)ethynyl)-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde

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Chemical Property of 4-(2-(5-(2-(4-(3,6-di-tert-butyl-9H-carbazolyl)phenyl)ethynyl)-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde

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Technology Process of 4-(2-(5-(2-(4-(3,6-di-tert-butyl-9H-carbazolyl)phenyl)ethynyl)-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde

There total 3 articles about 4-(2-(5-(2-(4-(3,6-di-tert-butyl-9H-carbazolyl)phenyl)ethynyl)-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde 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: 82.0%

: 1374843-67-0
4-(2-(5-bromo-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde

: 255829-44-8
3,6-di-tert-butyl-9-(4-ethynyl-phenyl)-9H-carbazole

: 1374843-11-4
4-(2-(5-(2-(4-(3,6-di-tert-butyl-9H-carbazolyl)phenyl)ethynyl)-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In N,N-dimethyl-formamide; at 80 ℃; for 14h; Inert atmosphere;
DOI:10.1016/j.jphotochem.2011.08.001

Reference yield:

: 4805-22-5
5,5'-dibromo-2,2'-bisthiophene

: 1374843-11-4
4-(2-(5-(2-(4-(3,6-di-tert-butyl-9H-carbazolyl)phenyl)ethynyl)-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 80 °C / Inert atmosphere

2: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; N-ethyl-N,N-diisopropylamine; triphenylphosphine / N,N-dimethyl-formamide / 14 h / 80 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In N,N-dimethyl-formamide; 1: Sonogashira coupling / 2: Sonogashira coupling;
DOI:10.1016/j.jphotochem.2011.08.001

Reference yield:

: 63697-96-1
4-Ethynylbenzaldehyde

: 1374843-11-4
4-(2-(5-(2-(4-(3,6-di-tert-butyl-9H-carbazolyl)phenyl)ethynyl)-2,2'-bithiophen-5'-yl)ethynyl)benzaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 80 °C / Inert atmosphere

2: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; N-ethyl-N,N-diisopropylamine; triphenylphosphine / N,N-dimethyl-formamide / 14 h / 80 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In N,N-dimethyl-formamide; 1: Sonogashira coupling / 2: Sonogashira coupling;
DOI:10.1016/j.jphotochem.2011.08.001