(1-allyl-4,5,6,7-tetrahydro-1H-benzimidazole-2-yl)[4-methylphenyl]methanone

Base Information

Chemical Name:(1-allyl-4,5,6,7-tetrahydro-1H-benzimidazole-2-yl)[4-methylphenyl]methanone
CAS No.:840503-10-8
Molecular Formula:C₁₈H₂₀N₂O
Molecular Weight:280.37
Hs Code.:

Synonyms:(1-allyl-4,5,6,7-tetrahydro-1H-benzimidazole-2-yl)[4-methylphenyl]methanone

Suppliers and Price of (1-allyl-4,5,6,7-tetrahydro-1H-benzimidazole-2-yl)[4-methylphenyl]methanone

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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-allyl-4,5,6,7-tetrahydro-1H-benzimidazole-2-yl)[4-methylphenyl]methanone

Chemical Property:

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Technology Process of (1-allyl-4,5,6,7-tetrahydro-1H-benzimidazole-2-yl)[4-methylphenyl]methanone

There total 4 articles about (1-allyl-4,5,6,7-tetrahydro-1H-benzimidazole-2-yl)[4-methylphenyl]methanone 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%

: 1290176-49-6
C₁₅H₁₆N₂O

: 106-95-6
allyl bromide

: 840503-10-8
(1-allyl-4,5,6,7-tetrahydro-1H-benzimidazole-2-yl)[4-methylphenyl]methanone

Guidance literature:: With 18-crown-6 ether; potassium carbonate; In tetrahydrofuran; at 40 ℃;
DOI:10.1016/j.bmcl.2011.02.032

Reference yield:

: 3752-24-7
4,5,6,7-tetrahydro-1H-benzimidazole

: 840503-10-8
(1-allyl-4,5,6,7-tetrahydro-1H-benzimidazole-2-yl)[4-methylphenyl]methanone

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / pyridine / 40 °C

2: 18-crown-6 ether; potassium carbonate / tetrahydrofuran / 40 °C

With 18-crown-6 ether; potassium carbonate; triethylamine; In tetrahydrofuran; pyridine;
DOI:10.1016/j.bmcl.2011.02.032

Reference yield:

: 874-60-2
4-methyl-benzoyl chloride

: 840503-10-8
(1-allyl-4,5,6,7-tetrahydro-1H-benzimidazole-2-yl)[4-methylphenyl]methanone

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / pyridine / 40 °C

2: 18-crown-6 ether; potassium carbonate / tetrahydrofuran / 40 °C

With 18-crown-6 ether; potassium carbonate; triethylamine; In tetrahydrofuran; pyridine;
DOI:10.1016/j.bmcl.2011.02.032