HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873229Generated: October 26, 2026
Ethyl cyanoacetate → HCID 18688664, compound
https://huagongshe.com/reaction/1873229
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Propanedioic acid, 2-(3-chloro-4-nitrophenyl)-2-methyl-, 1,3-diethyl ester | HCID 12854241 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 18688664 | HCID 18688664 | 92% |
Reaction Steps
Diethyl 2-(3-chloro-4-nitrophenyl)-2-methylmalonate (119 mg, 0.36 mmol.), ethyl cyanoacetate (81 mg, 0.72 mmol.), powdery potassium carbonate (119 mg, 0.86 mmol.), and dimethyl sulfoxide (1 mL) were mixed and stirred at 80° C. for 2 hours. The reaction mixture was cooled to room temperature, and washed with diethyl ether after addition of water. The aqueous portion was made acidic by addition of 6N hydrochloric acid, and extracted with diethyl ether. The ether portion was washed successively with water and an aqueous saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was distilled off to give 133 mg (yield: 92%) of the desired compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06111115 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-a18f04806da7495b8871167670e70da0 |
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| Source note | uspto-grants-2000_08 |
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