4-tert-butyl-N-(3-(2-hydroxyethoxy)-2-(4-methylphenyl)phenyl)benzenesulfonamide

Base Information

Chemical Name:4-tert-butyl-N-(3-(2-hydroxyethoxy)-2-(4-methylphenyl)phenyl)benzenesulfonamide
CAS No.:374600-28-9
Molecular Formula:C₂₅H₂₉NO₄S
Molecular Weight:439.576
Hs Code.:

Synonyms:4-tert-butyl-N-(3-(2-hydroxyethoxy)-2-(4-methylphenyl)phenyl)benzenesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-tert-butyl-N-(3-(2-hydroxyethoxy)-2-(4-methylphenyl)phenyl)benzenesulfonamide

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Technology Process of 4-tert-butyl-N-(3-(2-hydroxyethoxy)-2-(4-methylphenyl)phenyl)benzenesulfonamide

There total 6 articles about 4-tert-butyl-N-(3-(2-hydroxyethoxy)-2-(4-methylphenyl)phenyl)benzenesulfonamide 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: 93.0%

: 374601-16-8
N-((6-(2-benzyloxyethoxy)-4'-methylbiphenyl)-2-yl)-4-tert-butylbenzenesulfonamide

: 374600-28-9
4-tert-butyl-N-(3-(2-hydroxyethoxy)-2-(4-methylphenyl)phenyl)benzenesulfonamide

Guidance literature:: With water; hydrogen; 10percent Pd/C; In ethanol; at 20 ℃; for 3h;
DOI:10.1021/jm0102304

Reference yield:

: 15084-51-2
4-tert-butylbenzenesulfonyl chloride

: 374600-28-9
4-tert-butyl-N-(3-(2-hydroxyethoxy)-2-(4-methylphenyl)phenyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / pyridine / 2 h / 20 °C

2: 93 percent / H₂; H₂O / 10percent Pd/C / ethanol / 3 h / 20 °C

With pyridine; water; hydrogen; 10percent Pd/C; In ethanol;
DOI:10.1021/jm0102304

Reference yield:

: 603-84-9
2-chloro-3-nitrophenol

: 374600-28-9
4-tert-butyl-N-(3-(2-hydroxyethoxy)-2-(4-methylphenyl)phenyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: 85 percent / PPh₃; DEAD / tetrahydrofuran / 2 h / 0 °C

2: 89 percent / PdCl₂(PPh₃)2 / dioxane / 4 h / 20 °C

3: 87 percent / Fe; 10percent aq. HCl / ethanol / 3.5 h / Heating

4: 100 percent / pyridine / 2 h / 20 °C

5: 93 percent / H₂; H₂O / 10percent Pd/C / ethanol / 3 h / 20 °C

With pyridine; bis-triphenylphosphine-palladium(II) chloride; water; hydrogen; iron; triphenylphosphine; diethylazodicarboxylate; 10percent Pd/C; In tetrahydrofuran; 1,4-dioxane; ethanol;
DOI:10.1021/jm0102304