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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744442Generated: November 1, 2026

Ethyl cyanoacetate → HCID 69507081, compound

https://huagongshe.com/reaction/1744442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantPiperidineHCID 8082—
Reactant3-MethoxybenzaldehydeHCID 11569—
ReactantSodium hydrideHCID 24758—
Reactant1H-indol-4-olHCID 75421—
Reactant3-(3-Methoxyphenyl)-2-cyano-acrylic acid ethyl esterHCID 367497—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 69507081HCID 695070810.9%

Reaction Steps

To a solution of 3-methoxybenzaldehyde (2.0 g, 15.0 mmol) and ethyl cyanoacetate (1.56 mL, 15.0 mmol) in ethanol (10 mL) was added piperidine (0.73 ml, 7.5 mmol). The mixture was stirred at room temperature overnight. The solvent was evaporated and the crude oil was used for the next step. To a solution of 4-hydroxyindole (266.3 mg, 2 mmol) in toluene (5 mL) was added sodium hydride (100 mg, 2.5 mmol, 60%) and the mixture was stirred at room temperature for 0.5 h. To the mixture was added the 3-(3-methoxy-phenyl)-2-cyano-acrylic acid ethyl ester (462.5 mg, 2 mmol) dissolved in toluene (1 mL), then the mixture was refluxed for 2 h. The solvent was evaporated and the residue was purified by chromatography on silica gel with ethyl acetate and hexane (1:2) as eluant, yielding 6 mg (0.9%) the title compound. 1H NMR (CDCl3): 8.67 (brs, 1H), 7.54-7.48 (m, 1H), 7.35-7.31 (m, 2H), 7.15-7.01 (m, 5H), 3.88 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015328B2
Source datasetuspto-grants-2006_03
ORD IDord-4650369ad23f4182b9133136d8e5c326
Source noteuspto-grants-2006_03