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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095787Generated: November 1, 2026

Ethyl Acetate → HCID 66968962, compound

https://huagongshe.com/reaction/2095787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantSodium BicarbonateHCID 516892—
ReactantPyridine, 2-(4-fluorophenyl)-3-methyl-, 1-oxideHCID 58158491—
CatalystDimethylcarbamoyl ChlorideHCID 6598—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66968962HCID 6696896267%

Reaction Steps

To a solution of 2-(4-fluorophenyl)-3-methylpyridine 1-oxide (24 g, 0.118 mol) in tetrahydrofuran (200 mL) were added trimethylsilyl cyanide (19.2 mL, 0.153 mol) and dimethylcarbamoyl chloride (14.1 mL, 0.153 mmol), and the mixture was heated under reflux for 2 hr. Ethyl acetate and saturated aqueous sodium hydrogen carbonate solution were added to the reaction mixture, and the mixture was extracted 3 times with ethyl acetate. The combined organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtered, and the solvent was evaporated under reduced pressure. The obtained residue was washed with diethyl ether and collected by filtration to give the title compound (16.7 g, 67%) as a white solid. Under reduced pressure, the filtrate was concentrated, and the obtained residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/9) to give the title compound (3.0 g, 12%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445509B2
Source datasetuspto-grants-2013_05
ORD IDord-4dc3b516af8d4bd69533e8fa2be28354
Source noteuspto-grants-2013_05