Benzenesulfonamide, 4-methyl-N-(1-propylpentyl)-

Base Information

Chemical Name:Benzenesulfonamide, 4-methyl-N-(1-propylpentyl)-
CAS No.:90786-22-4
Molecular Formula:C15H25NO2S
Molecular Weight:283.435
Hs Code.:

Synonyms:

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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 Benzenesulfonamide, 4-methyl-N-(1-propylpentyl)-

Chemical Property:

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Technology Process of Benzenesulfonamide, 4-methyl-N-(1-propylpentyl)-

There total 2 articles about Benzenesulfonamide, 4-methyl-N-(1-propylpentyl)- 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:

: 111-66-0,25068-25-1
oct-1-ene

: 70-55-3
toluene-4-sulfonamide

: 81330-00-9
4-methyl-N-(octan-2-yl)benzenesulfonamide

: 90786-22-4
N-(octan-4-yl)-4-methyl-benzenesulfonamide

: N-(1-ethylhexyl)-4-methylbenzenesulfonamide

Guidance literature:: With (triphenyl phosphite)gold(I) chloride; silver trifluoromethanesulfonate; at 85 ℃; for 14h; Inert atmosphere; Darkness; neat (no solvent);
DOI:10.1002/adsc.201100478

Reference yield:

: 14850-23-8
trans-4-Octene

: 70-55-3
toluene-4-sulfonamide

: 90786-22-4
N-(octan-4-yl)-4-methyl-benzenesulfonamide

Guidance literature:: With sodium tetrahydroborate; mercury(II) nitrate; N-butylamine; Yield given. Multistep reaction; 1.) methylene dichloride, reflux, 24 h, 2.) aq. sodium hydroxide;

Reference yield: 68.0%

: 90786-22-4
N-(octan-4-yl)-4-methyl-benzenesulfonamide

: 124920-18-9
2-methyl-5-propyl-1-tosylpyrrolidine

Guidance literature:: With copper(l) iodide; bis-[(trifluoroacetoxy)iodo]benzene; In 1,2-dichloro-ethane; at 100 ℃; for 10h;
DOI:10.1039/c7cc02624b