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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304912Generated: November 2, 2026

Acetic Acid → HCID 178497377, compound

https://huagongshe.com/reaction/2304912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 178524171HCID 178524171—
CatalystRhodiumHCID 23948—
SolventMethanolHCID 887—
ProductHCID 178497377HCID 17849737792%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a 350 ml steel autoclave with teflon insert was placed 1H-benzimidazole-5-carboxylic acid (10 g, 61.7 mmol), 50% aqueous acetic acid (160 ml), 35% aqueous HCl solution (7 ml) and 6 g Rh/C (5%). The reaction mixture was hydrogenated at 60 bar H2 at 120° C. for 24 hours. After cooling and filtration through Celite, the filtrate was evaporated to dryness and the residue further dried under reduced pressure. The residue was mixed with methanol (200 ml) and (9 ml, 0.123 mol) thionyl chloride and heated at 80° C. for 2 hours. After cooling, the reaction mixture was evaporated to dryness and the white solid further dried under reduced pressure to yield 13.6 g (92%) of 4,5,6,7-tetrahydro-1H-benzimidazole-5-carboxylic acid methyl ester hydrochloride. The hydrochloride was treated with saturated sodium hydrogen carbonate solution (300 ml) and extracted with DCM (3×300 ml) to obtain 10.8 g (81%) of 4,5,6,7-tetrahydro-1H-benzimidazole-5-carboxylic acid methyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437147B1
Source datasetuspto-grants-2002_08
ORD IDord-191ec7b555164004a370db6a618e4fe5
Source noteuspto-grants-2002_08