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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059678Generated: October 25, 2026

Ammonium Acetate → 1-(4-Aminopiperidin-1-yl)-3-phenylpropan-1-one

https://huagongshe.com/reaction/1059678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-(3-Phenylpropionyl)-4-ketopiperidineHCID 17817612—
SolventMethanolHCID 887—
Product1-(4-Aminopiperidin-1-yl)-3-phenylpropan-1-oneHCID 1679377247%

Reaction Steps

To 3.2 g (13.8 mmol) of 135 in 125 mL of anhydrous methanol was added 21.3 g of ammonium acetate and 20 g of 3A molecular sieves. After stirring 30 min, 3.47 g (55.2 mmol) of sodium cyanoborohydride was added portionwise with stirring. After 3 hours, the mixture was gravity filtered, and the methanol evaporated under vacuum. The residue was partitioned between ice/HCl and ether. The acidic aqueous phase was extracted twice more with ether. The aqueous phase was made basic with ice and 50% aqueous NaOH. The mixture was extracted with CH2Cl2, dried, and evaporated under vacuum to give 1.5 g (47%) of the title amine 136. GC/MS indicated 100% purity with a molecular ion of 232.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521622B1
Source datasetuspto-grants-2003_02
ORD IDord-00b43c1f6c564e99953d86921cd77417
Source noteuspto-grants-2003_02