1-(dibenzo[b,d]furan-2-yl(phenyl)methyl)-3-butyl-1H-imidazol-3-ium iodide

Base Information

Chemical Name:1-(dibenzo[b,d]furan-2-yl(phenyl)methyl)-3-butyl-1H-imidazol-3-ium iodide
CAS No.:1449604-53-8
Molecular Formula:C₂₆H₂₅N₂O*I
Molecular Weight:508.402
Hs Code.:

Synonyms:1-(dibenzo[b,d]furan-2-yl(phenyl)methyl)-3-butyl-1H-imidazol-3-ium iodide

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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 1-(dibenzo[b,d]furan-2-yl(phenyl)methyl)-3-butyl-1H-imidazol-3-ium iodide

Chemical Property:

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Technology Process of 1-(dibenzo[b,d]furan-2-yl(phenyl)methyl)-3-butyl-1H-imidazol-3-ium iodide

There total 6 articles about 1-(dibenzo[b,d]furan-2-yl(phenyl)methyl)-3-butyl-1H-imidazol-3-ium 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: 82.0%

: 542-69-8
1-iodo-butane

: 1449604-25-4
1-(dibenzo[b,d]furan-2-yl(phenyl)methyl)-1H-imidazole

: 1449604-53-8
1-(dibenzo[b,d]furan-2-yl(phenyl)methyl)-3-butyl-1H-imidazol-3-ium iodide

Guidance literature:: In acetone; toluene; at 20 ℃; Reflux;
DOI:10.1016/j.ejmech.2013.06.011

Reference yield:

: 132-64-9,214827-48-2
dibenzofuran

: 1449604-53-8
1-(dibenzo[b,d]furan-2-yl(phenyl)methyl)-3-butyl-1H-imidazol-3-ium iodide

Guidance literature:: Multi-step reaction with 5 steps

1: aluminum (III) chloride / chloroform / 3 h / 20 °C

2: methanol; sodium tetrahydroborate / dichloromethane / 4.33 h / 0 - 20 °C

3: triethylamine / dichloromethane / 12 h / 0 - 20 °C

4: acetonitrile / Reflux

5: acetone; toluene / 20 °C / Reflux

With methanol; aluminum (III) chloride; sodium tetrahydroborate; triethylamine; In dichloromethane; chloroform; acetone; toluene; acetonitrile; 1: |Friedel-Crafts Acylation;
DOI:10.1016/j.ejmech.2013.06.011

Reference yield:

: 6407-29-0
1-(dibenzo[b,d]furan-2-yl)(phenyl)methanone

: 1449604-53-8
1-(dibenzo[b,d]furan-2-yl(phenyl)methyl)-3-butyl-1H-imidazol-3-ium iodide

Guidance literature:: Multi-step reaction with 4 steps

1: methanol; sodium tetrahydroborate / dichloromethane / 4.33 h / 0 - 20 °C

2: triethylamine / dichloromethane / 12 h / 0 - 20 °C

3: acetonitrile / Reflux

4: acetone; toluene / 20 °C / Reflux

With methanol; sodium tetrahydroborate; triethylamine; In dichloromethane; acetone; toluene; acetonitrile;
DOI:10.1016/j.ejmech.2013.06.011