HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → 4-(1-phenethyl-1H-benzoimidazol-2-ylmethyl)-benzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | methyl 4-((1H-benzo[d]imidazol-2-yl)methyl)benzoate | HCID 59468704 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(1-phenethyl-1H-benzoimidazol-2-ylmethyl)-benzoic acid methyl ester | HCID 58970783 | 30% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A solution of methyl 4-((1H-benzo[d]imidazol-2-yl)methyl)benzoate (200 mg, 0.75 mmol) in acetonitrile was treated with (2-bromoethyl)benzene (209 mg, 1.13 mmol) and potassium carbonate (143 mg, 0.90 mmol). The reaction mixture was heated with microwave irradiation at 100° C. for 2 h. The solvent was removed under reduced pressure and the residue was partitioned between water and dichloromethane. The organic phase was separated, dried over sodium sulfate and concentrated in vacuo. Purification of the resultant residue by flash column chromatography (silica, petroleum ether:ethyl acetate 8:2 to 1:1) afforded 4-(1-phenethyl-1H-benzoimidazol-2-ylmethyl)-benzoic acid methyl ester (30%). [M+H] 371.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820825B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-5fb8cc03dd4f43a7975b149e513880c5 |
| Source note | uspto-grants-2010_10 |