HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl cyanoacetate → Ethyl 4-acetamido-alpha-cyanocinnamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Acetamidobenzaldehyde | HCID 73942 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-acetamido-alpha-cyanocinnamate | HCID 245851 | 41.3% |
Reaction Steps
A mixture of 33.9 g (0.3 mol) of ethyl cyanoacetate and 59.1 g (0.3 mol) of 4-acetamidobenzaldehyde in 300 ml of ethanol in the presence of 5 ml of piperidine is refluxed for 3 hours. The very viscous medium is diluted with 800 ml of hot ethanol. It is filtered while hot. The yellow solid obtained is washed with hot ethanol. After filtration and drying, 32 g (41% yield) of ethyl 3-(4-acetylaminophenyl)-2-cyanoacrylate are obtained in the form of a pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06749839B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-c3920152b35949dc83c01c3200927c64 |
| Source note | uspto-grants-2004_06 |