HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Cyanoacetylethylcarbamate → ethyl N-(2-cyano-3-ethoxyacryloyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Cyanoacetylethylcarbamate | HCID 23112 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | ethyl N-(2-cyano-3-ethoxyacryloyl)carbamate | HCID 230015 | — |
Reaction Steps
A mixture of N-ethoxycarbonylcyanoacetamide (42 g), triethylorthoformate (40 g) and acetic anhydride (100 ml) is heated at reflux for one hour. The reaction is allowed to stand until cool and then is filtered, washing with ether, to yield α-cyano-β-ethoxy-N-ethoxycarbonylacrylamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04307098 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-ce1163e9f06b4b2cad154dcccf538134 |
| Source note | uspto-grants-1981_12 |