HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205293Generated: October 30, 2026
Sodium Carbonate → 3-(pyridin-4-yl)benzaldehyde
https://huagongshe.com/reaction/2205293
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Bromobenzaldehyde | HCID 76583 | — |
| Reactant | (Pyridin-4-yl)boronic acid | HCID 2734379 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Propan-2-ol--water (1/1) | HCID 21889133 | — |
| Product | 3-(pyridin-4-yl)benzaldehyde | HCID 2795563 | 67.4% |
Reaction Steps
Into a 2 L 3-necked round-bottom flask, purged and maintained with an inert atmosphere of nitrogen, was placed a solution of pyridin-4-ylboronic acid (30 g, 244 mmol, 1 equiv) in 2-propanol/water (800/40 mL), Na2CO3 (77.3 g, 729 mmol, 3 equiv), Pd(OAc)2 (5.46 g, 24.3 mmol, 0.1 equiv), PPh3 (12.75 g, 48.7 mmol, 0.2 equiv) and 3-bromobenzaldehyde (45 g, 243 mmol, 1 equiv). The mixture was stirred for 48 h at 80° C. in an oil bath. Then the solids were filtered out and the filtrate was concentrated under vacuum. The residue was purified by column chromatography on silica gel (eluting with 1:1 ethyl acetate/petroleum ether) to give 30 g of 3-(pyridin-4-yl)benzaldehyde as orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371285B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-7f66f8008bf34783b0ce3da21ab6e398 |
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| Source note | uspto-grants-2016_06 |
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