HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanoacetamide → alpha-Cyano-beta-(2-Nitro-4-Fluorophenyl)Acrylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanoacetamide | HCID 7898 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Fluoro-2-nitrobenzaldehyde | HCID 76226 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | alpha-Cyano-beta-(2-Nitro-4-Fluorophenyl)Acrylamide | HCID 54446537 | — |
Reaction Steps
A mixture of 4-fluoro-2-nitrobenzaldehyde (8.70 g., 51.5 millimoles), 2-cyanoacetamide (4.7 g., 54.4 millimoles), piperidine (0.032 g., 0.37 millimole) and ethanol (80 ml.) is stirred at room temperature for 28 hours. The solid which formed is separated by filtration, washed with ethanol (45 ml.) and dried. Yield = 10 g. (83.5%) of the title acrylamide as light tan crystals. M.P. 278°-279° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04044134 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-a91e5837ae214bbd83be559b5da9a343 |
| Source note | uspto-grants-1977_08 |