HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715932Generated: October 30, 2026
Dimethylformamide → 4-Chloro-5-fluoropyridine-3-carbaldehyde
https://huagongshe.com/reaction/715932
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 4-Chloro-3-fluoropyridine | HCID 3852429 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Chloro-5-fluoropyridine-3-carbaldehyde | HCID 71742306 | — |
Reaction Steps
4-Chloro-3-fluoropyridine (1 g) was dissolved in tetrahydrofuran (15 ml), and the solution was then cooled to −78° C. Lithium diisopropylamide (1.1 M solution in tetrahydrofuran and n-hexane, 7.6 ml) was added dropwise thereto, and the mixture was stirred at the same temperature as above for 5 hours. Then, N,N-dimethylformamide (1 ml) was added thereto, and the mixture was further stirred for 30 minutes while being heated to room temperature. Saturated saline was added to the reaction solution, followed by extraction with ethyl acetate. The extract was washed with water and saturated saline in this order and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel chromatography (n-hexane-ethyl acetate) to obtain the title compound (521 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09187489B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-b04ae81d28414ccd935165ee28c34685 |
|---|
| Source note | uspto-grants-2015_11 |
|---|