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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175688Generated: October 29, 2026

2-Hydroxy benzimidazole → HCID 67889876, compound

https://huagongshe.com/reaction/2175688

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Hydroxy benzimidazoleHCID 11985—
ReactantSodium hydrideHCID 24758—
Reactant(2E)-3-(3,4-dimethoxyphenyl)prop-2-enoyl chlorideHCID 11806394—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
ProductHCID 67889876HCID 6788987698.7%

Reaction Steps

To a solution of 1H-benzo[d]imidazol-2(3H)-one (268 mg, 2 mmol) in DMF (10 mL) at 0° C. was added 60% oily sodium hydride (88 mg, 2.2 mmol). When hydrogen evolution had ceased, a solution of (E)-3-(3,4-dimethoxyphenyl)acryloyl chloride (240 mg, 0.75 mmol) in DMF (3 mL) was added and the reaction mixture allowed to warm to room temperature and stirred for 1 hour. The reaction was quenched by addition of 1N hydrochloric acid, and extracted with DCM. The combined organic phases were washed with brine and dried over sodium sulfate. After concentration under reduced pressure, the residue was purified by flash column (hexane-EtOAc, 25:10) to give (E)-1-(3-(3,4-dimethoxyphenyl)acryloyl)-1H-benzo[d]imidazol-2(3H)-one (240 mg, 37%). LC-MS (ES-API); rt 9.02 min; m/z calculated for C18H16N2O4 [M+H]+ 325.1, found 325.0 and 347.0 ([M+Na]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062076B2
Source datasetuspto-grants-2015_06
ORD IDord-4ffe7068b8de48d0a94418700011c093
Source noteuspto-grants-2015_06