HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064964Generated: October 27, 2026
Nitrogen → 6-(2-Methyl-1,3-dioxolan-2-yl)-2-pyridinecarboxaldehyde
https://huagongshe.com/reaction/2064964
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Bromo-6-(2-methyl-1,3-dioxolan-2-yl)pyridine | HCID 12164282 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 6-(2-Methyl-1,3-dioxolan-2-yl)-2-pyridinecarboxaldehyde | HCID 86085920 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), to a solution of 2-bromo-6-(2-methyl-[1,3]dioxolan-2-yl)-pyridine (2.21 g, 9.05 mmol) in Et2O (60.0 mL) at −78° C. was added dropwise n-BuLi (3.70 mL of a 2.5M solution in hexane, 9.25 mmol). The reaction mixture was then stirred at −78° C. for 30 min before DMF (0.85 mL, 11.00 mmol) was added dropwise. The reaction mixture was allowed to warm to rt over 1 h. 5% aq. NaHCO3 was added and the mixture was extracted three times with Et2O. The combined org. extracts were dried over Na2SO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (4:1 hept-EA to pure EA) gave the title compound as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08288419B2 |
|---|
| Source dataset | uspto-grants-2012_10 |
|---|
| ORD ID | ord-00c723701142415ca5fca446fe7c609b |
|---|
| Source note | uspto-grants-2012_10 |
|---|