HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(4-fluorophenyl)prop-2-enamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-fluorophenyl)prop-2-enamide | HCID 3250203 | 100% |
Reaction Steps
4-Fluoroaniline (7 ml) and acryloyl chloride (7.2 ml) were dissolved in tetrahydrofuran (100 ml), then triethylamine (15 ml) was added thereto, and the mixture was stirred overnight at room temperature. The organic layer was partitioned by adding aqueous saturated sodium bicarbonate and ethyl acetate, and the organic layer was washed with water and dried over sodium sulfate anhydrous, and after the drying agent was filtered off, the filtrate was evaporated, whereby the title compound (12.2g, 100%) was obtained as pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06737425B1 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-e0bbd3078ba7473eaa022dca29988c67 |
| Source note | uspto-grants-2004_05 |