HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534775Generated: October 28, 2026
Methanol → 6-(Methylamino)nicotinaldehyde
https://huagongshe.com/reaction/534775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Dibah | HCID 16682954 | — |
| Reactant | 6-(Methylamino)pyridine-3-carbonitrile | HCID 17860899 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-(Methylamino)nicotinaldehyde | HCID 18416298 | — |
Reaction Steps
To 6-(methylamino)-3-pyridinecarbonitrile (D94) (0.1 g, 0.752 mmol) in toluene (10 mL) cooled to −78 C under argon was added Dibal-H (1.88 mL, 1M solution in toluene, 11.2 mmol) dropwise. The reaction was stirred at −78° C. and then allowed to warm to room temperature overnight. MeOH (0.47 mL) and 2 M H2SO4 (1.42 mL) were added and mixture was stirred for 1.5 h then concentrated in vacuo. The residue was partitioned between water and EtOAc. The aqueous layer was extracted with EtOAc and the combined organic layers were dried and concentrated to give the title compound (0.067 g). δH (CDCl3, 400 MHz) 9.78 (1H, s), 8.52 (1H, d), 7.92 (1H, dd), 6.45 (1H, d), 5.38 (1H, br.s), 3.04 (3H, d). MS (ES): MH+ 137.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853218B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-055b213759f34416bed1dfd49fc46710 |
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| Source note | uspto-grants-2014_10 |
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