HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → (2E)-3-(3-Bromophenyl)-N-ethyl-2-propenamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | trans 3-Bromocinnamoyl chloride | HCID 14959106 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (2E)-3-(3-Bromophenyl)-N-ethyl-2-propenamide | HCID 688145 | — |
Reaction Steps
A solution of trans 3-bromocinnamoyl chloride (12.3 g) in anhydrous toulene (150 ml) was added slowly with stirring to a solution of ethylamine (10 g) in dry ether (100 ml) at room temperature. The reaction mixture was heated at reflux for 1 hour, and the solvent and excess amine were then removed under reduced pressure. The residue was triturated with water, filtered, and recrystallized from ethanol-water to give trans 3-bromo-N-ethylcinnamamide, m.p. 89°-90° C., as a white crystalline material. NMR and IR spectra as well as elemental analysis were consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04041071 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-0b21772bad724033905ed838f46683e4 |
| Source note | uspto-grants-1977_08 |