HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanoacetamide → alpha-Cyano-beta-(2-Nitro-5-Fluorophenyl)Acrylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanoacetamide | HCID 7898 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 5-Fluoro-2-nitrobenzaldehyde | HCID 587090 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | alpha-Cyano-beta-(2-Nitro-5-Fluorophenyl)Acrylamide | HCID 53864188 | — |
Reaction Steps
A mixture of 3-fluoro-6-nitrobenzaldehyde (10.0 g., 0.0592 mole), 2-cyanoacetamide (5.24 g., 0.0622 mole), piperidine (0.37 g., 4.36 millimole) and ethanol (92 ml.) is heated to reflux on a steam bath for 2 hours. It is then cooled in an ice-bath whereupon the product precipitates and is recovered by filtration, washed with cold ethanol and dried. Yield = 9.1 g. (65%) of crude product. M.P. 162°-166° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04120962 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-2978c5c8d47b466e8e1317ca553d243f |
| Source note | uspto-grants-1978_10 |