HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354125Generated: October 27, 2026
Hydrochloric Acid → 2-Cyano-3-(3,4-dihydroxy-5-nitrophenyl)-N,N-diethylprop-2-enamide
https://huagongshe.com/reaction/2354125
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Entacapone Impurity 9 | HCID 67020297 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Cyano-3-(3,4-dihydroxy-5-nitrophenyl)-N,N-diethylprop-2-enamide | HCID 4659568 | 98% |
Reaction Steps
A round-bottom flask under nitrogen atmosphere is loaded with N,N-diethyl-2-cyano-3-(-3-methoxy-4-hydroxy-5-nitrophenyl-)-acrylamide (134 g, 0.421 mol) dissolved in dichloromethane (0.65 l) and triethylamine (128 g, 1.26 mol). The solution is cooled to 0-5° C. and aluminium trichloride (67.4 g, 0.505 mol) is added in portions. After that, the mixture is refluxed for 3-4 hours, until completion of the conversion. The reaction mixture is cooled to 0-5° C., a 20% hydrochloric acid solution (0.5 l) is dropped in the mixture, which is left under stirring at room temperature for 30 minutes. The resulting solid is filtered, washing with water (0.1 l×3), and dried in a static dryer under reduced pressure at 50° C.; 126 g are obtained. Yield: 98%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750177B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-33cc1b1e47c64f6395eff947ab093315 |
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| Source note | uspto-grants-2010_07 |
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