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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865256Generated: October 31, 2026

Ammonium Acetate → 4-Amino-1-benzyl-3-ethyl-3-methylpiperidine

https://huagongshe.com/reaction/1865256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 22278904HCID 22278904—
SolventMethanolHCID 887—
Product4-Amino-1-benzyl-3-ethyl-3-methylpiperidineHCID 22278895—

Reaction Conditions

Temperature0 °C

Reaction Steps

Ammonium acetate (2.5 g, 32.46 mmol) was added to the stirred solution of 1-benzyl-3-ethyl-3-methyl-4-piperidinone (0.9 g, 3.9 mmol) in methanol (20 ml) and stirring was continued for 3 hr at ambient temperature. The resulting mixture was cooled at 0° C. and sodium cyanoborohydride (0.2 g, 3.1 mmol) was added to it. Cooling was removed after 10 min. and resulting mixture was stirred for 6 hr at ambient temperature. The reaction mixture was concentrated to dryness, triturated with water, acidified with conc. HCl (pH 3˜4) and extracted with ethyl acetate to remove impurities. The aqueous layer was basified with 1 M sodium hydroxide solution (pH10) and extracted with ethyl acetate. Ethyl acetate extract was dried (Na2SO4) and concentrated to dryness to furnish 4-amino-1-benzyl-3-ethyl-3-methylpiperidine. Yield 0.6 g (66%), C15H24N2, m/z 233 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07626032B2
Source datasetuspto-grants-2009_12
ORD IDord-02c863b1f2d3444096f4e52dcb329f3e
Source noteuspto-grants-2009_12