HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814487Generated: October 31, 2026
3-Bromopyridine → 3-Bromopyridine-4-carboxaldehyde
https://huagongshe.com/reaction/1814487
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromopyridine | HCID 12286 | — |
| Reactant | N-Formylmorpholine | HCID 20417 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | LDA cyclohexane | HCID 86604122 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Bromopyridine-4-carboxaldehyde | HCID 2762997 | 40% |
Reaction Steps
3-Bromopyridine (1.582 g) was dissolved in tetrahydrofuran (20 ml), followed by the addition of a 1.5M solution of lithium diisopropylamide/cyclohexane (7.3 ml) in nitrogen atmosphere at −70° C., and the resulting mixture was stirred for 5 min. Continuously, 4-formylmorpholine (3 ml) was added thereto and stirred for 20 min, followed by the further stirring at room temperature for 30 min. An aqueous solution of saturated ammonium chloride was added to the reaction mixture, and then it was extracted with ethyl acetate. The resulting organic layer was washed with water, dried (over MgSO4) and evaporated. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane system), to give the title compound as a colorless solid (749 mg, yield; 40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06875761B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-4008616c772c4d3c85b759cc7f1eac4e |
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| Source note | uspto-grants-2005_04 |
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