HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016010Generated: October 30, 2026
Dimethylformamide → 6-Bromo-3-pyridinecarboxaldehyde
https://huagongshe.com/reaction/1016010
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Bromo-3-pyridinecarboxaldehyde | HCID 11769234 | 37.6% |
Reaction Steps
2,5-Dibromopyridine 9.48 g (40 mmol) was dissolved in 60 mL of THF and 150 mL of anhydrous ether. After the solution was cooled to −78° C., 16 mL of n-butyllithium (2.5 M, 40 mmol) was slowly dropped through a syringe in 30 min. After being stirred at −78° C. for 30 minutes, N,N-dimethylformamide (3.5 g, 48 mmol) was added. The reaction mixture was warmed up to room temperature during two hours and then quenched by addition of 10 mL of water. The mixture was extracted twice using EtOAc. The combined extracts were dried and concentrated. After flash column using 30-40% EtOAc in hexane, 2.80 g of white solid was obtained (28% yield), MS: 186.0, 188.0 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985730B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-fbe344d4c52d4a0d8c9e6a8b53bdd5f3 |
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| Source note | uspto-grants-2011_07 |
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