HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7161Generated: October 25, 2026
Dimethylformamide → 2-Fluoropyridine-3-carbaldehyde
https://huagongshe.com/reaction/7161
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Fluoropyridine | HCID 9746 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Fluoropyridine-3-carbaldehyde | HCID 11434944 | 15% |
Reaction Steps
A solution of 2-fluoropyridine (306 mg, 3.15 mmol) in THF (1 mL) was added to a solution of lithium diisopropylamide in THF (0.20 M, 17 mL, 3.4 mmol) at −78° C. The solution was stirred at −78° C. for 4 h, then DMF (0.73 mL, 9.4 mmol) was added dropwise and stirring was continued at −78° C. for 2.5 h. Saturated NH4Cl(aq) (2 mL) was added, and the mixture was allowed to warm to room temperature. The mixture was diluted with EtOAc (20 mL), and the organic phase was washed with saturated NaHCO3(aq) (20 mL) and brine (10 mL), then dried (MgSO4) and concentrated in vacuo. Purification of the crude material by chromatography on silica gel (10% EtOAc/hexanes) gave the title compound as a yellow liquid (58 mg, 15%). 1H NMR (CDCl3) □ 7.39 (m, 1H), 8.32 (m, 1H), 8.48 (m, 1H), 10.33 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07084155B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-ae7961b104604450beaed78f4ad54709 |
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| Source note | uspto-grants-2006_08 |
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