HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 3-[4-fluoro-2-(trifluoromethyl)phenyl]prop-2-enoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Malonic Acid | HCID 867 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Fluoro-2-(trifluoromethyl)benzaldehyde | HCID 522940 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-[4-fluoro-2-(trifluoromethyl)phenyl]prop-2-enoic Acid | HCID 2737583 | 49% |
Reaction Steps
A mixture of 4-Fluoro-2-trifluoromethyl-benzaldehyde (2 g, 10.2 mmol), malonic acid (1.2 g, 11.2 mmol), piperidine (0.087 g, 1 mmol) and pyridine (7 ml) was kept at reflux temperature until carbon dioxide formation ceased (3 h). After cooling to room temperature the reaction mixture was poured onto 40 g ice and 20 ml 6N HCl. The precipitate was isolated, washed with water and dried yielding 1.16 g (49%) 3-(4-fluoro-2-trifluoromethyl-phenyl)-acrylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07205326B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-cfc43d38416345dd9e55146ed08ca7dc |
| Source note | uspto-grants-2007_04 |