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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400184Generated: November 3, 2026

Ethyl cyanoacetate → HCID 49788127, compound

https://huagongshe.com/reaction/1400184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Bromoacetyl)pyridine hydrobromideHCID 2776239—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 49788127HCID 4978812787.3%

Reaction Steps

To a suspension of sodium metal (81 mg, 3.5 mmol) in 10 mL anhydrous EtOH, ethylcyanoacetate (0.37 mL, 3.5 mmol) was added at 0° C. The solution was stirred until sodium was completely dissolved. The solvent was evaporated to obtain a white solid that was added portionwise to a stirred solution of bromoacetylpyridine 1 (1.0 g, 3.5 mmol) in anhydrous THF (20 mL) and DIEA (0.6 mL, 3.5 mmol). The reaction mixture was stirred overnight at rt. The solvent was removed, the residue was suspended in water and extracted with DCM. The organic extracts were dried over Na2SO4 and concentrated. The crude was purified by flash chromatography (DCM/MeOH 95:5) to give 710 mg (87%) of 2-cyano-4-oxo-4-pyridin-4-yl-butyric acid ethyl ester as a reddish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906934B2
Source datasetuspto-grants-2014_12
ORD IDord-ca958c2e681541ecb2f3ae14383ce519
Source noteuspto-grants-2014_12