HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454932Generated: October 30, 2026
Dimethylformamide → 5-Bromo-4-methylpyridine-3-carbaldehyde
https://huagongshe.com/reaction/1454932
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3,5-Dibromo-4-methylpyridine | HCID 819338 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 5-Bromo-4-methylpyridine-3-carbaldehyde | HCID 22238337 | — |
Reaction Steps
Under argon, an n-butyllithium solution in hexane (1.55N, 4.6 ml) is added dropwise to a 3,5-dibromo-4-methylpyridine solution (intermediate 10.1, 1.76 g, 7 mmol) kept at −100° C. After stirring for 5 min, DMF (0.84 ml, 1.54 equiv.) is added dropwise. The stirring is maintained for 20 min at −100° C. and then for 1 h at −78° C. An aqueous NH4Cl solution is added and the reaction mixture is extracted with a diethyl ether/water mixture. The yellow solid obtained is purified on silica gel (100 g), eluting with AcOEt/petroleum ether (1/4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07482342B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-0077a2d412244a438f2a6e1f82095496 |
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| Source note | uspto-grants-2009_01 |
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