HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxygen → Ethyl 3-phenylprop-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Propionic Acid | HCID 1032 | — |
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Acrylate | HCID 25188 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | Ethyl 3-phenylprop-2-enoate | HCID 7649 | — |
Reaction Steps
In a flask, 30 mmol of bromobenzene, 1.5 mmol of ethyl acrylate, 0.1 mmol of palladium(II) acetate, 0.02 mmol of H7PMo8V4O40, 0.08 mmol of sodium acetate, 0.1 mmol of acetylacetone, and 5 ml of propionic acid were placed and were stirred at a constant temperature of 90° C. in an atmosphere of oxygen gas at 1 atm (0.1 MPa) for 7 hours. The resulting reaction mixture was analyzed by gas chromatography to find that ethyl 3-[(o, m, or p)-bromophenyl]acrylate (o-isomer:m-isomer:p-isomer=38:35:27) and ethyl cinnamate were produced in yields of 49% and 4%, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07414160B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-262d50cae0964f2fadb1b6fbdb481b66 |
| Source note | uspto-grants-2008_08 |