HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-Ethenyl-6-fluoro-2-methylbenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-Bromo-6-fluoro-2-methylbenzonitrile | HCID 66643852 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Product | 3-Ethenyl-6-fluoro-2-methylbenzonitrile | HCID 66643866 | — |
Reaction Steps
3-Bromo-6-fluoro-2-methylbenzonitrile (23.6 g, 110 mmol), potassium vinyl trifluoroborate (29.5 g, 221 mmol), PdCl2(dppf)-CH2Cl2 Adduct (4.03 g, 5.51 mmol), and TEA (30.7 mL, 221 mmol) were added to 250 mL of ethanol. The reaction mixture was degassed then stirred at reflux for 4 h. LC-MS confirmed the presence of product. The reaction mixture was diluted with ethyl acetate, washed twice with brine, dried, and evaporated to dryness. The crude material was then purified by MPLC chromatography using a 330 g Redi-sep column and eluting with a 10% EtOAc/Hexane solvent system to yield 3-ethenyl-6-fluoro-2-methylbenzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062070B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-07f42805eeff41c796d12765556246f3 |
| Source note | uspto-grants-2015_06 |