5-tert-butyl-2-<2-(2-methoxyethoxy)-5-nitrobenzenesulfonamido>-1,4-benzoquinone

Base Information

Chemical Name:5-tert-butyl-2-<2-(2-methoxyethoxy)-5-nitrobenzenesulfonamido>-1,4-benzoquinone
CAS No.:84011-57-4
Molecular Formula:C₁₉H₂₂N₂O₈S
Molecular Weight:438.458
Hs Code.:

Synonyms:5-tert-butyl-2-<2-(2-methoxyethoxy)-5-nitrobenzenesulfonamido>-1,4-benzoquinone

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Chemical Property of 5-tert-butyl-2-<2-(2-methoxyethoxy)-5-nitrobenzenesulfonamido>-1,4-benzoquinone

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Technology Process of 5-tert-butyl-2-<2-(2-methoxyethoxy)-5-nitrobenzenesulfonamido>-1,4-benzoquinone

There total 5 articles about 5-tert-butyl-2-<2-(2-methoxyethoxy)-5-nitrobenzenesulfonamido>-1,4-benzoquinone 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: 71.0%

: 84011-50-7
5-tert-butyl-4-(hexadecyloxy)-N-<<2-(2-methoxyethoxy)-5-nitrophenyl>sulfonyl>-o-benzoquinone imine

: 84011-57-4
5-tert-butyl-2-<2-(2-methoxyethoxy)-5-nitrobenzenesulfonamido>-1,4-benzoquinone

Guidance literature:: With hydrogenchloride; In methanol; for 0.5h; Ambient temperature;
DOI:10.1021/jo00150a008

Reference yield:

: 69920-06-5
2-(2-Methoxyethoxy)-5-nitrobenzenesulfonyl chloride

: 84011-57-4
5-tert-butyl-2-<2-(2-methoxyethoxy)-5-nitrobenzenesulfonamido>-1,4-benzoquinone

Guidance literature:: Multi-step reaction with 3 steps

2: 62 percent / MnO₂ / acetone / 1.5 h / Ambient temperature

3: 71 percent / 35percent HCl / methanol / 0.5 h / Ambient temperature

With hydrogenchloride; manganese(IV) oxide; In methanol; acetone;
DOI:10.1021/jo00150a008

Reference yield:

: 78819-50-8
2-amino-5-tert-butyl-4-(hexadecyloxy)phenol hydrochloride

: 84011-57-4
5-tert-butyl-2-<2-(2-methoxyethoxy)-5-nitrobenzenesulfonamido>-1,4-benzoquinone

Guidance literature:: Multi-step reaction with 3 steps

2: 62 percent / MnO₂ / acetone / 1.5 h / Ambient temperature

3: 71 percent / 35percent HCl / methanol / 0.5 h / Ambient temperature

With hydrogenchloride; manganese(IV) oxide; In methanol; acetone;
DOI:10.1021/jo00150a008