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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40842Generated: October 26, 2026

Ammonium Acetate → tert-Butyl 4-(1-aminoethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/40842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-Acetyl-piperidine-1-carboxylic acid tert-butyl esterHCID 10987983—
SolventMethanolHCID 887—
SolventSodium HydroxideHCID 14798—
Producttert-Butyl 4-(1-aminoethyl)piperidine-1-carboxylateHCID 2264729590%

Reaction Steps

A mixture of tert-butyl 4-acetylpiperidine-1-carboxylate (145 g, 0.64 mol) and ammonium acetate (225 g, 2.9 mol) in methanol (2 L) was stirred at room temperature for 1.5 hours. Sodium cyanoborohydride (30 g, 0.48 mol) was added in one portion and the stirring was continued overnight at room temperature. The reaction mixture was poured in 2N aq. NaOH (2 L) and extracted with dichloromethane (2×1 L). The combined extracts were washed with water (1 L), brine (0.3 L), and evaporated to dryness. The residue was dissolved in TBME (1.5 L), dried over sodium sulfate, filtered, and evaporated to dryness under reduced pressure. The residue was purified by bulb to bulb distillation at 180° C. and 0.1 mbar to afford the title compound as a colorless oil that partly solidified upon standing (131 g, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530489B2
Source datasetuspto-grants-2013_09
ORD IDord-369371af84394b78a597fa75f03191d5
Source noteuspto-grants-2013_09