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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970715Generated: November 1, 2026

Chloroacetic Acid → 2-(Chloromethyl)-1-methylbenzimidazole

https://huagongshe.com/reaction/1970715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetic AcidHCID 300—
ReactantHydrochloric AcidHCID 313—
ReactantBenzenamine, N-methyl-2-nitro-HCID 69157—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-(Chloromethyl)-1-methylbenzimidazoleHCID 24804477.9%

Reaction Steps

To a pressure reaction bottle was added 4 g N-methyl-2-nitroaniline, 0.44 g 5% palladium on carbon, and 100 ml ethanol. The mixture was hydrogenated at 22 C and 40 psi hydrogen for 2 hours. Following filtration through celite, and solvent removal, a dark red oil was obtained. To this oil was added 3.7 g chloroacetic acid and 40 ml 5M hydrochloric acid. After refluxing under nitrogen for 2.5 hours, the mixture was cooled to 22 C, diluted with 200 ml water, and neutralized with solid sodium bicarbonate. The resulting solid was filtered, washed with water and dried giving 3.7 g gray solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431045B2
Source datasetuspto-grants-2013_04
ORD IDord-9a014a98b713493681fc6e3dcb842638
Source noteuspto-grants-2013_04