HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Methyl 1-benzyl-1H-benzimidazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | methyl 1H-1,3-benzodiazole-5-carboxylate | HCID 2779733 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 1-benzyl-1H-benzimidazole-5-carboxylate | HCID 54450488 | 22.2% |
Reaction Steps
A mixture of 2.8 g of methyl 5-benzimidazolecarboxylate (prepared as described in Preparation 26), 3.52 g of benzyl bromide, 3 g of potassium carbonate and 50 ml of acetone was stirred for 3 days at room temperature. At the end of this time, the solvent was removed by evaporation under reduced pressure and the residue was mixed with an aqueous solution of sodium chloride, after which it was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue was then recrystallized from a mixture of ethyl acetate and hexane, to give 0.94 g of the title compound, melting at 156°-162° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05886014 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-ba3e220a895f48f4abeccf9969b9d70b |
| Source note | uspto-grants-1999_03 |