4-(4-benzoylphenoxy)-N-(3-(5-(dimethylamino)naphthalene-1-sulfonamido)propyl)-N,N-dimethylbutan-1-ammonium iodide

Base Information

Chemical Name:4-(4-benzoylphenoxy)-N-(3-(5-(dimethylamino)naphthalene-1-sulfonamido)propyl)-N,N-dimethylbutan-1-ammonium iodide
CAS No.:1572037-55-8
Molecular Formula:C₃₄H₄₂N₃O₄S*I
Molecular Weight:715.696
Hs Code.:

Synonyms:4-(4-benzoylphenoxy)-N-(3-(5-(dimethylamino)naphthalene-1-sulfonamido)propyl)-N,N-dimethylbutan-1-ammonium iodide

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Chemical Property of 4-(4-benzoylphenoxy)-N-(3-(5-(dimethylamino)naphthalene-1-sulfonamido)propyl)-N,N-dimethylbutan-1-ammonium iodide

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Technology Process of 4-(4-benzoylphenoxy)-N-(3-(5-(dimethylamino)naphthalene-1-sulfonamido)propyl)-N,N-dimethylbutan-1-ammonium iodide

There total 4 articles about 4-(4-benzoylphenoxy)-N-(3-(5-(dimethylamino)naphthalene-1-sulfonamido)propyl)-N,N-dimethylbutan-1-ammonium iodide 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: 56.9%

: 178666-16-5
4-O-(4-iodobutyl)benzophenone

: 30003-07-7
5-(dimethylamino)-N-(3-(dimethylamino)propyl)naphthalene-1-sulfonamide

: 1572037-55-8
4-(4-benzoylphenoxy)-N-(3-(5-(dimethylamino)naphthalene-1-sulfonamido)propyl)-N,N-dimethylbutan-1-ammonium iodide

Guidance literature:: In acetonitrile; at 100 ℃; for 24h; Temperature; Time;
DOI:10.1039/c3tb21633k

Reference yield:

4-[(4-bromobutyl)oxy]benzophenone: 101308-54-7
4-[(4-bromobutyl)oxy]benzophenone

: 1572037-55-8
4-(4-benzoylphenoxy)-N-(3-(5-(dimethylamino)naphthalene-1-sulfonamido)propyl)-N,N-dimethylbutan-1-ammonium iodide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium iodide / acetone / 24 h / Reflux

2: acetonitrile / 24 h / 100 °C

With sodium iodide; In acetone; acetonitrile; 2: |Menshutkin Reaction;
DOI:10.1039/c3tb21633k

Reference yield:

: 1137-42-4
4-Hydroxybenzophenone

: 1572037-55-8
4-(4-benzoylphenoxy)-N-(3-(5-(dimethylamino)naphthalene-1-sulfonamido)propyl)-N,N-dimethylbutan-1-ammonium iodide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / acetonitrile / 24 h / Reflux

2: sodium iodide / acetone / 24 h / Reflux

3: acetonitrile / 24 h / 100 °C

With potassium carbonate; sodium iodide; In acetone; acetonitrile; 3: |Menshutkin Reaction;
DOI:10.1039/c3tb21633k