2-{4-[2-(2-{5-[2-(2-{4-[bis-(4-tert-butyl-phenyl)-(4-ethyl-phenyl)-methyl]-phenoxy}-ethoxy)-ethoxy]-naphthalen-1-yloxy}-ethoxy)-ethylsulfanyl]-5-ethylsulfanyl-[1,3]dithiol-2-ylidene}-5H-[1,3]dithiolo[4,5-c]pyrrole

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Chemical Name:2-{4-[2-(2-{5-[2-(2-{4-[bis-(4-tert-butyl-phenyl)-(4-ethyl-phenyl)-methyl]-phenoxy}-ethoxy)-ethoxy]-naphthalen-1-yloxy}-ethoxy)-ethylsulfanyl]-5-ethylsulfanyl-[1,3]dithiol-2-ylidene}-5H-[1,3]dithiolo[4,5-c]pyrrole
CAS No.:846571-65-1
Molecular Formula:C₆₃H₆₉NO₅S₆
Molecular Weight:1112.64
Hs Code.:

2-{4-[2-(2-{5-[2-(2-{4-[bis-(4-<i>tert</i>-butyl-phenyl)-(4-ethyl-phenyl)-methyl]-phenoxy}-ethoxy)-ethoxy]-naphthalen-1-yloxy}-ethoxy)-ethylsulfanyl]-5-ethylsulfanyl-[1,3]dithiol-2-ylidene}-5<i>H</i>-[1,3]dithiolo[4,5-<i>c</i>]pyrrole

Synonyms:2-{4-[2-(2-{5-[2-(2-{4-[bis-(4-tert-butyl-phenyl)-(4-ethyl-phenyl)-methyl]-phenoxy}-ethoxy)-ethoxy]-naphthalen-1-yloxy}-ethoxy)-ethylsulfanyl]-5-ethylsulfanyl-[1,3]dithiol-2-ylidene}-5H-[1,3]dithiolo[4,5-c]pyrrole

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Chemical Property of 2-{4-[2-(2-{5-[2-(2-{4-[bis-(4-tert-butyl-phenyl)-(4-ethyl-phenyl)-methyl]-phenoxy}-ethoxy)-ethoxy]-naphthalen-1-yloxy}-ethoxy)-ethylsulfanyl]-5-ethylsulfanyl-[1,3]dithiol-2-ylidene}-5H-[1,3]dithiolo[4,5-c]pyrrole

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Technology Process of 2-{4-[2-(2-{5-[2-(2-{4-[bis-(4-tert-butyl-phenyl)-(4-ethyl-phenyl)-methyl]-phenoxy}-ethoxy)-ethoxy]-naphthalen-1-yloxy}-ethoxy)-ethylsulfanyl]-5-ethylsulfanyl-[1,3]dithiol-2-ylidene}-5H-[1,3]dithiolo[4,5-c]pyrrole

There total 4 articles about 2-{4-[2-(2-{5-[2-(2-{4-[bis-(4-tert-butyl-phenyl)-(4-ethyl-phenyl)-methyl]-phenoxy}-ethoxy)-ethoxy]-naphthalen-1-yloxy}-ethoxy)-ethylsulfanyl]-5-ethylsulfanyl-[1,3]dithiol-2-ylidene}-5H-[1,3]dithiolo[4,5-c]pyrrole 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: 87.0%

: 846571-63-9
2-{4-[2-(2-{5-[2-(2-{4-[bis-(4-tert-butyl-phenyl)-(4-ethyl-phenyl)-methyl]-phenoxy}-ethoxy)-ethoxy]-naphthalen-1-yloxy}-ethoxy)-ethylsulfanyl]-5-ethylsulfanyl-[1,3]dithiol-2-ylidene}-5-(toluene-4-sulfonyl)-5H-[1,3]dithiolo[4,5-c]pyrrole

: 846571-65-1
2-{4-[2-(2-{5-[2-(2-{4-[bis-(4-tert-butyl-phenyl)-(4-ethyl-phenyl)-methyl]-phenoxy}-ethoxy)-ethoxy]-naphthalen-1-yloxy}-ethoxy)-ethylsulfanyl]-5-ethylsulfanyl-[1,3]dithiol-2-ylidene}-5H-[1,3]dithiolo[4,5-c]pyrrole

Guidance literature:: With sodium methylate; In tetrahydrofuran; methanol; for 0.25h; Heating;
DOI:10.1021/jp0448494 DOI:10.1002/chem.200500934

Reference yield:

: 153530-55-3
2-(2-{5-[2-(2-toluene-4-sulfonyloxy-ethoxy)-ethoxy]-naphthalen-1-yloxy}-ethoxy)-ethoxysulfonyl-4-toluene

: 846571-65-1
2-{4-[2-(2-{5-[2-(2-{4-[bis-(4-tert-butyl-phenyl)-(4-ethyl-phenyl)-methyl]-phenoxy}-ethoxy)-ethoxy]-naphthalen-1-yloxy}-ethoxy)-ethylsulfanyl]-5-ethylsulfanyl-[1,3]dithiol-2-ylidene}-5H-[1,3]dithiolo[4,5-c]pyrrole

Guidance literature:: Multi-step reaction with 3 steps

1.1: 86 percent / K₂CO₃ / acetonitrile / 84 h / Heating

2.1: 97 percent / NaI / acetone / 40 h / Heating

3.1: CsOH*H₂O / tetrahydrofuran; methanol / 22.5 h / 20 °C

3.2: tetrahydrofuran; methanol / 24 h / 20 °C

3.3: 56 percent / NaOMe / tetrahydrofuran; methanol / 0.42 h / Heating

With cesium hydroxide; potassium carbonate; sodium iodide; In tetrahydrofuran; methanol; acetone; acetonitrile;
DOI:10.1002/chem.200204589

Reference yield:

: 177609-49-3
bis(4-tert-butylphenyl)(4-ethylphenyl)(4-hydroxyphenyl)methane

: 846571-65-1
2-{4-[2-(2-{5-[2-(2-{4-[bis-(4-tert-butyl-phenyl)-(4-ethyl-phenyl)-methyl]-phenoxy}-ethoxy)-ethoxy]-naphthalen-1-yloxy}-ethoxy)-ethylsulfanyl]-5-ethylsulfanyl-[1,3]dithiol-2-ylidene}-5H-[1,3]dithiolo[4,5-c]pyrrole

Guidance literature:: Multi-step reaction with 3 steps

1.1: 86 percent / K₂CO₃ / acetonitrile / 84 h / Heating

2.1: 97 percent / NaI / acetone / 40 h / Heating

3.1: CsOH*H₂O / tetrahydrofuran; methanol / 22.5 h / 20 °C

3.2: tetrahydrofuran; methanol / 24 h / 20 °C

3.3: 56 percent / NaOMe / tetrahydrofuran; methanol / 0.42 h / Heating

With cesium hydroxide; potassium carbonate; sodium iodide; In tetrahydrofuran; methanol; acetone; acetonitrile;
DOI:10.1002/chem.200204589