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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716843Generated: November 2, 2026

Methyl iodide → Methyl 4-((1-Methyl-1H-benzimidazol-2-yl)methyl)benzoate

https://huagongshe.com/reaction/1716843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactantmethyl 4-((1H-benzo[d]imidazol-2-yl)methyl)benzoateHCID 59468704—
SolventAcetoneHCID 180—
ProductMethyl 4-((1-Methyl-1H-benzimidazol-2-yl)methyl)benzoateHCID 5946870628%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of methyl 4-((1H-benzimidazol-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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803825B2
Source datasetuspto-grants-2010_09
ORD IDord-86ed945bd34c4312a35736767fe9c231
Source noteuspto-grants-2010_09