N-methyl-N-[3-(4'-iodophenoxy)-1-propyl]N,N,N-trimethylammonium 4-methylbenzenesulfonate

Base Information

Chemical Name:N-methyl-N-[3-(4'-iodophenoxy)-1-propyl]N,N,N-trimethylammonium 4-methylbenzenesulfonate
CAS No.:1389265-01-3
Molecular Formula:C₇H₇O₃S*C₁₂H₁₉INO
Molecular Weight:491.39
Hs Code.:

Synonyms:N-methyl-N-[3-(4'-iodophenoxy)-1-propyl]N,N,N-trimethylammonium 4-methylbenzenesulfonate

Suppliers and Price of N-methyl-N-[3-(4'-iodophenoxy)-1-propyl]N,N,N-trimethylammonium 4-methylbenzenesulfonate

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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 N-methyl-N-[3-(4'-iodophenoxy)-1-propyl]N,N,N-trimethylammonium 4-methylbenzenesulfonate

Chemical Property:

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Technology Process of N-methyl-N-[3-(4'-iodophenoxy)-1-propyl]N,N,N-trimethylammonium 4-methylbenzenesulfonate

There total 4 articles about N-methyl-N-[3-(4'-iodophenoxy)-1-propyl]N,N,N-trimethylammonium 4-methylbenzenesulfonate 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: 99.0%

: 1008460-14-7
C₁₆H₁₇IO₄S

: 1389265-01-3
N-methyl-N-[3-(4'-iodophenoxy)-1-propyl]N,N,N-trimethylammonium 4-methylbenzenesulfonate

Guidance literature:: In acetonitrile; at 60 ℃;
DOI:10.1055/s-0031-1290766

Reference yield:

: 145073-42-3
3-(4-iodophenoxy)propan-1-ol

: 1389265-01-3
N-methyl-N-[3-(4'-iodophenoxy)-1-propyl]N,N,N-trimethylammonium 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine; trimethylamine hydrochloride / dichloromethane / 1.5 h / 0 °C

2: dichloromethane; water; tetrahydrofuran / 24 h / 20 °C

3: dichloromethane / 4 h / 20 °C

With trimethylamine hydrochloride; triethylamine; In tetrahydrofuran; dichloromethane; water;
DOI:10.1016/j.tet.2013.02.017

Reference yield:

: 540-38-5
p-Iodophenol

: 1389265-01-3
N-methyl-N-[3-(4'-iodophenoxy)-1-propyl]N,N,N-trimethylammonium 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 4 steps

1: potassium iodide; potassium carbonate / N,N-dimethyl-formamide / 6 h / Reflux

2: triethylamine; trimethylamine hydrochloride / dichloromethane / 1.5 h / 0 °C

3: dichloromethane; water; tetrahydrofuran / 24 h / 20 °C

4: dichloromethane / 4 h / 20 °C

With trimethylamine hydrochloride; potassium carbonate; triethylamine; potassium iodide; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2013.02.017