HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Bromo-2-fluoro-3-methoxybenzaldehyde → 2-Fluoro-3-methoxy-6-vinylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Bromo-2-fluoro-3-methoxybenzaldehyde | HCID 23157915 | — |
| Reactant | Potassium vinyltrifluoroborate | HCID 23679353 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | 2-Fluoro-3-methoxy-6-vinylbenzaldehyde | HCID 57722773 | — |
Reaction Steps
To a stirred solution of 6-bromo-2-fluoro-3-methoxybenzaldehyde (13 g, 56 mmol) in nPrOH (200 mL) were added potassium vinyltrifluoroborate (7.9 g, 59 mmol), PdCl2(dppf) (0.91 g, 1.1 mmol), and TEA (7.8 mL, 56 mmol). The reaction mixture was purged with N2 for 10 min, heated to reflux for 3 h, cooled to room temperature, treated with water, and concentrated. The residue was extracted with EtOAc (×3). The combined organics were washed with brine, dried (Na2SO4), concentrated, and purified by flash chromatography to afford the title compound. 1H NMR (600 MHz, CDCl3) δ 10.53 (s, 1H); 7.43 (dd, 1H); 7.31 (d, 1H); 7.16 (t, 1H); 5.60 (d, 1H); 5.36 (d, 1H); 3.95 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07550478B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-42d8d05eba7d410494dbb9a287c1de5c |
| Source note | uspto-grants-2009_06 |