(6-benzoyl-2-thioxo-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl)-phenyl-methanone

Base Information

Chemical Name:(6-benzoyl-2-thioxo-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl)-phenyl-methanone
CAS No.:785777-30-2
Molecular Formula:C₁₉H₁₂O₂S₅
Molecular Weight:432.633
Hs Code.:

Synonyms:(6-benzoyl-2-thioxo-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl)-phenyl-methanone

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Chemical Property of (6-benzoyl-2-thioxo-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl)-phenyl-methanone

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Technology Process of (6-benzoyl-2-thioxo-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl)-phenyl-methanone

There total 1 articles about (6-benzoyl-2-thioxo-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl)-phenyl-methanone 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: 63.0%

: 85931-57-3,123399-69-9
1,3-dithiol-2,4,5-trithione

: 959-28-4
1,4-diphenylbut-2-ene-1,4-dione

: 785777-30-2
(6-benzoyl-2-thioxo-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl)-phenyl-methanone

Guidance literature:: In toluene; for 2h; Heating;
DOI:10.1039/b404545a

Reference yield: 55.0%

: 785777-30-2
(6-benzoyl-2-thioxo-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl)-phenyl-methanone

: 785777-33-5
2,5-diphenylthienodithiino[3,4-b:5,6-e]1,3-dithiole-2-thione

Guidance literature:: With tetraphosphorus decasulfide; sodium hydrogencarbonate; In 1,4-dioxane; at 90 ℃; for 2h;
DOI:10.1039/b404545a

Reference yield:

: 785777-30-2
(6-benzoyl-2-thioxo-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl)-phenyl-methanone

: 785777-36-8
2,5-diphenylthienodithiino[3,4-b:5,6-e]1,3-dithiole-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 55 percent / P₂S₅; NaHCO₃ / dioxane / 2 h / 90 °C

2: 76 percent / Hg(OAc)2; AcOH / CH₂Cl₂ / 5 h / 20 °C

With tetraphosphorus decasulfide; mercury(II) diacetate; sodium hydrogencarbonate; acetic acid; In 1,4-dioxane; dichloromethane;
DOI:10.1039/b404545a