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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110810Generated: November 3, 2026

Methyl 2-methylbenzimidazole-5-carboxylate hydrochloride → Methyl 2-methyl-4,5,6,7-tetrahydro-1H-benzo[d]imidazole-6-carboxylate

https://huagongshe.com/reaction/1110810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-methylbenzimidazole-5-carboxylate hydrochlorideHCID 22154382—
CatalystPalladium barium sulphateHCID 17887766—
SolventAcetic AcidHCID 176—
ProductMethyl 2-methyl-4,5,6,7-tetrahydro-1H-benzo[d]imidazole-6-carboxylateHCID 1079789012%

Reaction Steps

In an autoclave 6.8 g (30 mmols) of methyl 2-methylbenzimidazole-5-carboxylate hydrochloride, 6.0 g of 5% palladium-barium sulfate and 140 ml of acetic acid were charged and hydrogenation was carried out at 80° C. for 115 hours under 60 atms with stirring. After cooling, 5% palladium-barium sulfate was filtered off and the filtrate was distilled off under reduced pressure. After 200 ml of water was added to the residue, 1 N sodium hydroxide solution was added to the mixture at 0° to 5° C. to adjust pH to 9 to 10 followed by extraction with ethyl acetate. The ethyl acetate layer was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography and eluted with methylene chloride-methanol (10 : 1) to give 0.70 g (12.0%) of methyl 2-methyl-4,5,6,7-tetrahydrobenzimidazole-5-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977175
Source datasetuspto-grants-1990_12
ORD IDord-3b666d317a6945f8b69ffc0b82f44ec5
Source noteuspto-grants-1990_12