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3-{[5-tert-butylsulfanyl-3-(2',3'-dinitro-4'-trimethylsilylethynylphenyl)ethynyl]phenylethynyl}-3'-(5-tert-butylsulfanyl-2-iodophenylethynyl)tolane

Base Information
  • Chemical Name:3-{[5-tert-butylsulfanyl-3-(2',3'-dinitro-4'-trimethylsilylethynylphenyl)ethynyl]phenylethynyl}-3'-(5-tert-butylsulfanyl-2-iodophenylethynyl)tolane
  • CAS No.:914673-94-2
  • Molecular Formula:C51H43IN2O4S2Si
  • Molecular Weight:967.035
  • Hs Code.:
3-{[5-tert-butylsulfanyl-3-(2',3'-dinitro-4'-trimethylsilylethynylphenyl)ethynyl]phenylethynyl}-3'-(5-tert-butylsulfanyl-2-iodophenylethynyl)tolane

Synonyms:3-{[5-tert-butylsulfanyl-3-(2',3'-dinitro-4'-trimethylsilylethynylphenyl)ethynyl]phenylethynyl}-3'-(5-tert-butylsulfanyl-2-iodophenylethynyl)tolane

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Chemical Property of 3-{[5-tert-butylsulfanyl-3-(2',3'-dinitro-4'-trimethylsilylethynylphenyl)ethynyl]phenylethynyl}-3'-(5-tert-butylsulfanyl-2-iodophenylethynyl)tolane
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Technology Process of 3-{[5-tert-butylsulfanyl-3-(2',3'-dinitro-4'-trimethylsilylethynylphenyl)ethynyl]phenylethynyl}-3'-(5-tert-butylsulfanyl-2-iodophenylethynyl)tolane

There total 13 articles about 3-{[5-tert-butylsulfanyl-3-(2',3'-dinitro-4'-trimethylsilylethynylphenyl)ethynyl]phenylethynyl}-3'-(5-tert-butylsulfanyl-2-iodophenylethynyl)tolane 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 7 steps
1.1: 76 percent / dimethylformamide / 1 h / 20 °C
2.1: 95 percent / aq. HCl / methanol / 1 h / 60 °C
3.1: 89 percent / Et3N / CH2Cl2 / 1 h / 0 °C
4.1: 88 percent / Pd(PPh3)4; CuI; triethylamine / tetrahydrofuran / 4 h / 20 °C
5.1: 95 percent / aq. HCl; tin / tetrahydrofuran / 1 h / 20 °C
6.1: BF3*Et2O; tert-BuONO / tetrahydrofuran / 0.5 h / -20 - -5 °C
6.2: 38 percent / KI; I2 / acetonitrile; H2O; CH2Cl2 / 16 h / 20 °C
7.1: 23 percent / Pd(PPh3)4; CuI; (iPr)2NEt / toluene / 24 h / 20 °C
With hydrogenchloride; tin; copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); tert.-butylnitrite; boron trifluoride diethyl etherate; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; toluene; 4.1: Sonogashira coupling / 7.1: Sonogashira coupling;
DOI:10.1002/ejoc.200600336
Guidance literature:
Multi-step reaction with 6 steps
1.1: 95 percent / aq. HCl / methanol / 1 h / 60 °C
2.1: 89 percent / Et3N / CH2Cl2 / 1 h / 0 °C
3.1: 88 percent / Pd(PPh3)4; CuI; triethylamine / tetrahydrofuran / 4 h / 20 °C
4.1: 95 percent / aq. HCl; tin / tetrahydrofuran / 1 h / 20 °C
5.1: BF3*Et2O; tert-BuONO / tetrahydrofuran / 0.5 h / -20 - -5 °C
5.2: 38 percent / KI; I2 / acetonitrile; H2O; CH2Cl2 / 16 h / 20 °C
6.1: 23 percent / Pd(PPh3)4; CuI; (iPr)2NEt / toluene / 24 h / 20 °C
With hydrogenchloride; tin; copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); tert.-butylnitrite; boron trifluoride diethyl etherate; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; toluene; 3.1: Sonogashira coupling / 6.1: Sonogashira coupling;
DOI:10.1002/ejoc.200600336
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