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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381013Generated: November 1, 2026

Ammonia → 4-(3-Methylpyridin-2-YL)butan-1-amine

https://huagongshe.com/reaction/1381013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2,3-LutidineHCID 11420—
ReactantSodium amideHCID 24533—
Reactant1-Propanamine, 3-chloro-, hydrochlorideHCID 11469095—
SolventWaterHCID 962—
Product4-(3-Methylpyridin-2-YL)butan-1-amineHCID 2019596762.3%

Reaction Steps

2,3-Lutidine (321 g) was added with stirring to a solution of sodamide (351 g) in liquid ammonia (3 l ). 1-Amino-3-chloropropane hydrochloride (429 g) was added to this mixture over 8 minutes with stirring. Any liquid ammonia lost through evaporation was replaced. After 2 hours the reaction was quenched by the addition of ammonium chloride (120 g) and the reaction mixture was left to stand overnight to allow substantially complete escape of ammonia through evaporation. The residue so obtained was diluted with water (2 l) and extracted with dichloromethane. The extracts were dried (Na2SO4), the dichloromethane removed by evaporation and the residue distilled in vacuo to give 2-(4-aminobutyl)-3-methylpyridine (306.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04584381
Source datasetuspto-grants-1986_04
ORD IDord-2a6df57bb3ea4ab297cf23294f20909a
Source noteuspto-grants-1986_04