2-(4,4-dimethyl-2-oxoimidazolidin-1-yl)-N-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)-N,N-dimethylethanaminium 4-methylbenzenesulfonate

Base Information

Chemical Name:2-(4,4-dimethyl-2-oxoimidazolidin-1-yl)-N-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)-N,N-dimethylethanaminium 4-methylbenzenesulfonate
CAS No.:1373434-50-4
Molecular Formula:C₇H₇O₃S*C₁₆H₃₄N₃O₄
Molecular Weight:503.66
Hs Code.:

Synonyms:2-(4,4-dimethyl-2-oxoimidazolidin-1-yl)-N-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)-N,N-dimethylethanaminium 4-methylbenzenesulfonate

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Chemical Property of 2-(4,4-dimethyl-2-oxoimidazolidin-1-yl)-N-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)-N,N-dimethylethanaminium 4-methylbenzenesulfonate

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Technology Process of 2-(4,4-dimethyl-2-oxoimidazolidin-1-yl)-N-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)-N,N-dimethylethanaminium 4-methylbenzenesulfonate

There total 5 articles about 2-(4,4-dimethyl-2-oxoimidazolidin-1-yl)-N-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)-N,N-dimethylethanaminium 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:

: 1225437-87-5
1-(2-(dimethylamino)ethyl)-4,4-dimethylimidazolidin-2-one

: 62921-74-8,518012-62-9,58320-73-3
2-(2-(2-methoxyethoxy)ethoxy)ethyl p-toluenesulfonate

: 1373434-50-4
2-(4,4-dimethyl-2-oxoimidazolidin-1-yl)-N-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)-N,N-dimethylethanaminium 4-methylbenzenesulfonate

Guidance literature:: at 60 ℃; for 4.5h; Sealed tube;

Reference yield:

: 2-(2-nitro-2-methyl-propylamino)-ethanol

: 1373434-50-4
2-(4,4-dimethyl-2-oxoimidazolidin-1-yl)-N-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)-N,N-dimethylethanaminium 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogen / Raney nickel / water; methanol / 48 h / 23272.3 Torr

2: 0.75 h / 200 °C

3: pyridine / dichloromethane / 20 h / 20 °C

4: tetrahydrofuran / 8 h / 60 °C / Sealed tube

5: 4.5 h / 60 °C / Sealed tube

With pyridine; hydrogen; Raney nickel; In tetrahydrofuran; methanol; dichloromethane; water;

Reference yield:

: 1310681-19-6
1-(2-hydroxyethyl)-4,4-dimethylimidazolidin-2-one

: 1373434-50-4
2-(4,4-dimethyl-2-oxoimidazolidin-1-yl)-N-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)-N,N-dimethylethanaminium 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / dichloromethane / 20 h / 20 °C

2: tetrahydrofuran / 8 h / 60 °C / Sealed tube

3: 4.5 h / 60 °C / Sealed tube

With pyridine; In tetrahydrofuran; dichloromethane;