HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → 4-(3-Chloropyridin-2-yl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,3-Dichloropyridine | HCID 16988 | — |
| Reactant | 4-Formylphenylboronic Acid | HCID 591073 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4-(3-Chloropyridin-2-yl)benzaldehyde | HCID 53426238 | 81% |
Reaction Steps
{circle around (1)} 100 g (0.676 mol) of 2,3-dichloropyridine, 101.4 g (0.676 mol) of (4-formylphenyl)boronic acid and 86 g (0.811 mol) of sodium carbonate were dissolved in 500 mL of 1,2-dimethoxyethane and 500 mL of distilled water, and 78 g (0.0676 mol) of Pd(PPh3)4 was added. The mixture was heated to reflux for 18 hours so that it was allowed to react. After completion of the reaction, the reaction solution was concentrated under reduced pressure to remove 1,2-dimethoxyethane, and then extracted with ethyl acetate. The extract was treated with magnesium sulfate, filtered and concentrated under reduced pressure, yielding 4-(3-chloropyridin-2-yl)benzaldehyde as represented below in a 81% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040572B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-d521a4a5a4704322b0c7ee93df46e062 |
| Source note | uspto-grants-2015_05 |