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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1718421Generated: October 30, 2026

Sodium hydride → Ethyl 2-[(2'-cyanobiphenyl-4-yl)methyl]-3-oxohexanoate

https://huagongshe.com/reaction/1718421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 3-oxohexanoateHCID 238498—
Reactant4'-(Bromomethyl)-2-cyanobiphenylHCID 1501912—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-[(2'-cyanobiphenyl-4-yl)methyl]-3-oxohexanoateHCID 10020734100.5%

Reaction Steps

To a suspension of sodium hydride (60% in oil, 19.1 g) in tetrahydrofuran (500 ml) was added a solution of ethyl 3-oxohexanoate (116 g) in tetrahydrofuran (500 ml) dropwise at room temperature. After being stirred at room temperature for 30 min, 4′-(bromomethyl)-biphenyl-2-carbonitrile (100 g) was added to the mixture and the mixture was stirred at room temperature for 15 hr. Ethyl acetate and saturated aqueous ammonium chloride solution were added to the mixture. The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were successively washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound as a pale yellow oil (129 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803940B2
Source datasetuspto-grants-2010_09
ORD IDord-4462bd0269b94f70bc197c3e6dad3541
Source noteuspto-grants-2010_09