HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367679Generated: October 31, 2026
Diisobutylaluminum hydride → 5-Nitropyridine-2-carbaldehyde
https://huagongshe.com/reaction/2367679
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Methyl 5-nitropicolinate | HCID 12457882 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Nitropyridine-2-carbaldehyde | HCID 15145501 | 60% |
Reaction Steps
To a suspension of methyl 5-nitropicolinate (LIX) (1.282 g, 7.03 mmol) in DCM (25 mL) stirred at −78° C. under argon was slowly added DIBAL (1M in toluene) (9.14 mL, 9.14 mmol). The solution was allowed to warm to room temperature over 3 h. An aqueous solution of potassium sodium tartrate was added, diluted further with water and DCM. The solution was stirred at room temperature for another 30 min before the organic layer was separated. The aqueous layer was extracted 2×DCM, combined with the organic layer, dried over MgSO4, filtered and evaporated under reduced pressure. The residue was purified by column chromatography to produce 5-nitropicolinaldehyde (LX) as a brown oil (0.64 g, 4.2 mmol, 60% yield). 1H NMR (DMSO-d6) δ ppm 8.17 (d, J=9 Hz, 1H), 8.81 (dd, J=9 Hz, J=2 Hz, 1H), 9.56 (d, J=2 Hz, 1H), 10.08 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08697887B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-6b83dd15f9dc4ac9a8da14930289bbe5 |
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| Source note | uspto-grants-2014_04 |
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