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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747146Generated: October 30, 2026

Sodium hydride → HCID 58780780, compound

https://huagongshe.com/reaction/747146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-FluorobenzaldehydeHCID 68009—
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
Reactant5-Bromo-2-methoxypyridineHCID 2734895—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 58780780HCID 5878078029%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a suspension of sodium hydride (8.8 g, 0.220 mol) in 1,2-dimethoxyethane (300 ml) was added diethyl cyanomethylphosphonate (19.7 g, 0.122 mol) little by little at room temperature under an atmosphere of nitrogen gas. After stirring for 15 minutes, 5-bromo-2-methoxypyridine (20.0 g, 0.106 mol) and tetrakis(triphenylphosphine)palladium (0) (2.0 g, 1.73 mmol) were successively added thereto, followed by heating to 90° C. and stirring for 6 hours. The reaction mixture was cooled as it was and further ice-cooled. 3-Fluorobenzaldehyde (13.7 g, 0.110 mol) was added dropwise thereto over 1.5 hours at 1 to 4° C. under an atmosphere of nitrogen gas, followed by stirring further for 2.5 hours while gradually elevating to room temperature. The reaction mixture was diluted with a saturated aqueous ammonium chloride solution and ethyl acetate, and then the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with a saturated aqueous ammonium chloride solution twice, dried over anhydrous sodium sulfate and then concentrated. The residue was suspended in methanol, and then the resulting solid was collected by filtration and washed with diethyl ether and hexane, to give the title compound (7.80 g, 29%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396836B2
Source datasetuspto-grants-2008_07
ORD IDord-6111a449b76040c8836b89480a26f5a4
Source noteuspto-grants-2008_07