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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771310Generated: November 3, 2026

Acetaldehyde → N-Ethyl-6-methylpyridin-2-amine

https://huagongshe.com/reaction/1771310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
Reactant2-Amino-6-methylpyridineHCID 15765—
ReactantSodium triacetoxyborohydrideHCID 5049666—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductN-Ethyl-6-methylpyridin-2-amineHCID 301605151%

Reaction Steps

2-Amino-6-methylpyridine (1.00 g, 9.25 mmol) and acetaldehyde (0.52 mL, 9.34 mmol) were stirred together in anhydrous methyl alcohol for 1 hour at room temperature under a nitrogen atmosphere. The mixture was then treated with sodium triacetoxyborohydride (7.84 g, 37.0 mmol) and five drops of acetic acid and all was allowed to continue stirring for 4 hours. The reaction mixture was concentrated in vacuo. The residue was partitioned between water and DCM, and the separated aqueous phase was extracted twice with DCM. The combined organics were dried over MgSO4, filtered and concentrated in vacuo to give a mobile oil which was purified by flash column chromatography, eluting with 2% MeOH/DCM, to give 2-ethylamino-6-methylpyridine (636 mg, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249130B2
Source datasetuspto-grants-2016_02
ORD IDord-3913c5c40e4f4c62b4e450f0f4a3c8b7
Source noteuspto-grants-2016_02