HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → trans-Cinnamamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Acrylamide | HCID 6579 | — |
| Reactant | Acrylic Acid | HCID 6581 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | trans-Cinnamamide | HCID 5273472 | — |
Reaction Steps
Acrylic acid vii is converted to the acid chloride with oxalyl chloride, and the resulting acid chloride is reacted with an aniline in the presence of base. The resulting acrylamide viii is then reacted with an appropriately substituted aryl iodide ix in the presence of a palladium catalyst and a base to give the cinnamide vi.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07652041B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-a9f07c831d5d4cc7b7478445fb8fbec7 |
| Source note | uspto-grants-2010_01 |