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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723218Generated: October 30, 2026

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

https://huagongshe.com/reaction/1723218

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, IH, 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 numberUS04859692
Source datasetuspto-grants-1989_08
ORD IDord-db02119677a04ebc880d082b4d8c1aa2
Source noteuspto-grants-1989_08