HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allylamine → 3-fluoro-N-allylcinnamamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | HCID 2759064 | HCID 2759064 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-fluoro-N-allylcinnamamide | HCID 54515971 | — |
Reaction Steps
A solution of 3-fluorocinnamoyl chloride (3.7 g) in dry toluene (35 ml) was added with stirring to allylamine (8 ml) in dry benzene (100 ml). The reaction mixture was allowed to stand at room temperature for three days. After evaporation of the solvents under reduced pressure the residue was triturated with water containing a small amount of sodium carbonate and washed with water. Recrystallization from ethanol: water gave 3-fluoro-N-allylcinnamamide (3.3 g), m.p. 84.5-87° C. as fine white needles. Elemental analysis, nmr and ir spectra were consistent with the structure assignment.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04179524 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-8e16d01c7ffc413d9434011f51d17eab |
| Source note | uspto-grants-1979_12 |