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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673749Generated: October 29, 2026

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

https://huagongshe.com/reaction/1673749

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 numberUS07998968B2
Source datasetuspto-grants-2011_08
ORD IDord-8d516e898d204a2b871d2535ed5e54d5
Source noteuspto-grants-2011_08