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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637472Generated: November 1, 2026

1-(1H-Imidazol-1-yl)ethanone → HCID 19348510, compound

https://huagongshe.com/reaction/1637472

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1H-Imidazol-1-yl)ethanoneHCID 17174—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 19348416HCID 19348416—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 19348510HCID 19348510—

Reaction Steps

2.39 ml (1.19 mmol) of a 0.5 M potassium bis(trimethylsilyl)amide solution in toluene were added dropwise at room temperature over a period of 3 minutes to a solution of 338 mg (0.78 mmol) of N-(2-t-butyl-5-carbamoylphenyl)-3-(2-methoxyphenyl)octanamide (prepared as described in Example 151) in 5.0 ml of dry tetrahydrofuran, and the resulting mixture was stirred for 15 minutes, after which 175 mg (1.59 mmol) of 1-acetylimidazole were added. The reaction mixture was stirred for 40 minutes, after which it was diluted with ethyl acetate, and the diluted solution was washed with a saturated aqueous solution of potassium hydrogensulfate and with a saturated aqueous solution of sodium chloride, in that order. It was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through silica gel using a 1:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 363 mg (a quantitative yield) of the title compound as a colorless foam-like substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06040339
Source datasetuspto-grants-2000_03
ORD IDord-1ecda8529b6d473fbbbedb660e8731c4
Source noteuspto-grants-2000_03