HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163087Generated: October 28, 2026
Methyl iodide → Methyl 4-((1-Methyl-1H-benzimidazol-2-yl)methyl)benzoate
https://huagongshe.com/reaction/1163087
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | methyl 4-((1H-benzo[d]imidazol-2-yl)methyl)benzoate | HCID 59468704 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 4-((1-Methyl-1H-benzimidazol-2-yl)methyl)benzoate | HCID 59468706 | 28% |
Reaction Steps
A solution of methyl 4-((1H-benzo[d]imidazol-2-yl)methyl)benzoate (0.2 g, 0.75 mmol) in acetone was treated with potassium carbonate (0.31 g, 2.2 mmol), cooled to 0° C., treated dropwise with and methyl iodide (0.070 mL, 1.1 mmol), heated at 40° C. for 12 h, cooled to room temperature, and filtered. The filtrate was evaporated under reduced pressure. Purification of the resultant residue by column chromatography (silica, chloroform) afforded the title product (28%). 1H NMR (400 MHz, CDCl3): 7.98 (d, J=8.4 Hz, 2H), 7.7 (m, 1H), 7.37 (m,5H), 4.38 (s, 2H), 3.9 (s, 3H), 3.5 (s, 3H). [M+H] 281.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820825B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-42c45dc29a8646809c544ccce74584c4 |
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| Source note | uspto-grants-2010_10 |
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