HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanoacetamide → alpha-Cyano-beta-(2-Nitro-4,5-Dimethoxyphenyl)Acrylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanoacetamide | HCID 7898 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 6-Nitroveratraldehyde | HCID 88505 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | alpha-Cyano-beta-(2-Nitro-4,5-Dimethoxyphenyl)Acrylamide | HCID 4145653 | — |
Reaction Steps
Piperidine (2.1 g., 0.0237 mole) and 2-cyanoacetamide (22.0 g., 0.263 mole) are added to a slurry of 6-nitroveratraldehyde (50.0 g., 0.237 mole) in methanol (500 ml.). The mixture is heated to reflux for 2 hours, and then cooled in an ice bath and filtered. The bright yellow filter cake is washed with cold isopropanol (300 ml.) and then air dried. Yield = 60.1 g. (93%); m.p. 265°-266° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04044134 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-25c95626a215461da2793469a09d051f |
| Source note | uspto-grants-1977_08 |