HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775413Generated: October 28, 2026
Dimethylformamide → 4-Bromopyridine-3-carbaldehyde
https://huagongshe.com/reaction/1775413
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Bromopyridinium chloride | HCID 88100 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Bromopyridine-3-carbaldehyde | HCID 11116740 | 31.4% |
Reaction Steps
A suspension of 4-bromopyridine hydrochloride (5.0 g, 25.7 mmol) in THF (100 mL) was purged with N2 and cooled to −78° C. A solution of lithium diisopropylamide (2.0 M solution in heptane/THF/ethylbenzene, 27.0 mL, 54.0 mmol) was added over 3 minutes. After 30 minutes, DMF (8.56 mL, 110.6 mmol) was added. The reaction mixture was stirred at −78° C. for 15 minutes before rapidly warming to room temperature in a water bath. The reaction was allowed to stir at ambient temperature for 18 hours. The reaction was quenched with saturated NH4Cl (100 mL) and extracted with EtOAc. The combined organic extracts were washed with water and brine, dried over Na2SO4, evaporated, and chromatographed (Analogix 150 g silica gel column eluting with a gradient of 100% heptane 50% EtOAc/heptane over 1 hour) to give 1.50 g (31%) of the title compound as a light yellow solid. MS m/z 186 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260450B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-86caee2ece1e45d5b95c03e1eda39be4 |
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| Source note | uspto-grants-2016_02 |
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