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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275138Generated: October 26, 2026

Potassium Carbonate → Methyl 3-methoxy-4-(6-nitrobenzimidazol-1-ylmethyl)benzoate

https://huagongshe.com/reaction/275138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-(bromomethyl)-3-methoxybenzoateHCID 2759828—
ReactantHCID 178526486HCID 178526486—
SolventMethyl Ethyl KetoneHCID 6569—
ProductMethyl 3-methoxy-4-(6-nitrobenzimidazol-1-ylmethyl)benzoateHCID 1476309626%

Reaction Steps

A solution of 6-nitrobenzimidazole (2.0 g.) and methyl 4-bromomethyl-3-methoxybenzoate (B) (3.5 g.) in methyl ethyl ketone (61 ml.) was treated with potassium carbonate (1.9 g.) and then heated under reflux for 24 hours. The solvent was then evaporated. The residue was extracted with ethyl acetate and inorganic material removed by filtration. The filtrate was evaporated. The resultant residue was purified by flash chromatography on a 6×30 cm. silica gel column using 1:1 v/v hexane:ethyl acetate as the eluent to give methyl 3-methoxy-4-(6-nitrobenzimidazol-1-ylmethyl)benzoate (K) (1.07 g., 26%); NMR: 3.9 (s,3H, OCH3), 4.0(s,3H, OCH3), 5.7(s,2H, NCH2), 7.4(d, 1H, Ar), 7.8(d,1H, H4 -benzimidazole), 8.1(dd, 1H, H5 -benzimidazole), 8.6(br s,2H, H2,7 -benzimidazole).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05391758
Source datasetuspto-grants-1995_02
ORD IDord-ecbfbf910ddf4aa1a213530dcbce141c
Source noteuspto-grants-1995_02