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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909006Generated: October 30, 2026

Water → 1-(1H-Benzo[d]imidazol-4-yl)ethanone

https://huagongshe.com/reaction/1909006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
ReactantN-methoxy-N-methyl-1H-benzo[d]imidazole-4-carboxamideHCID 76845951—
ReactantHCID 178418348HCID 178418348—
SolventTetrahydrofuranHCID 8028—
Product1-(1H-Benzo[d]imidazol-4-yl)ethanoneHCID 1942595784%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of 1H-benzoimidazole-4-carboxylic acid methoxy-methyl-amide (742 mg, 3.62 mmol) in THF (36 mL) at −78° C. was added MeLi (1.6M; 2.49 mL, 3.98 mmol) dropwise. The mixture was stirred at −78° C. for 2 hours before an additional 1.0 mol. eq. MeLi (2.3 mL) was added dropwise. The mixture was stirred at −78° C. for a further 2 hours before saturated aqueous NH4Cl solution was added and the mixture warmed to room temperature. Enough water was added to dissolve all solids and the phases were separated. The aqueous phase was extracted into CHCl3 (×3), dried and concentrated in vacuo to give a white solid. Trituration with EtOAc (5 mL) followed by collection by filtration and washing with 4:1 Et2O/EtOAc (5 mL) provided 1-(1H-benzoimidazol-4-yl)-ethanone (487 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598217B2
Source datasetuspto-grants-2013_12
ORD IDord-28fa676edd9844aca0affd7cf6b86003
Source noteuspto-grants-2013_12