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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480739Generated: October 30, 2026

Ethyl cyanoacetate → HCID 13704246, compound

https://huagongshe.com/reaction/1480739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4-fluoro-3-nitrobenzoateHCID 5219721—
SolventHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 13704246HCID 13704246174.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 2-cyanoacetate (10.9 mL, 102 mmol) was slowly added to a 60% suspension of sodium hydride (4.10 g, 102 mmol) in N,N-dimethylformamide (125 mL) at 0° C. to give a gray suspension. The mixture was stirred at 0° C. for 15 minutes and methyl 4-fluoro-3-nitrobenzoate (10.2 g, 51 mmol) in N,N-dimethylformamide (125 mL) was added. The resulting deep red mixture was stirred at 0° C. for 30 minutes and at room temperature for 3 hours. The reaction mixture was diluted with 1N HCl (40 mL) and ethyl acetate (40 mL). The separated aqueous layer was extracted with ethyl acetate (3×50 mL). The organic layers were combined and dried over anhydrous sodium sulfate, filtered and concentrated to afford a residue (26 g) which was purified by flash-chromatography (started with 100% hexanes and gradually added ethyl acetate increments to complete with 100% ethyl acetate) to afford 14.9 g of the title compound. LCMS m/z 291.0 (M−H)−, retention time (on analytical HPLC)=1.76 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409906B2
Source datasetuspto-grants-2016_08
ORD IDord-270adbc4f1df455c827bad81940966ee
Source noteuspto-grants-2016_08