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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616368Generated: October 26, 2026

1-Benzyl-4-piperidone → N~1~-(1-Benzylpiperidin-4-yl)-N~2~-phenylethane-1,2-diamine

https://huagongshe.com/reaction/616368

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-piperidoneHCID 19220—
Reactant1,2-Ethanediamine, N1-phenyl-HCID 74270—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
ProductN~1~-(1-Benzylpiperidin-4-yl)-N~2~-phenylethane-1,2-diamineHCID 20540168—

Reaction Steps

To the solution of 12.6 g of N-phenylethylenediamine in 200 ml of methanol, 50 ml of 4.1 N ethanolic hydrogen chloride are added dropwise followed by 18.9 g of 1-benzyl-4-piperidone in 100 ml of methanol. Then, 9.45 g sodium cyanoborohydride are added in portions while stirring at room temperature. After 72 hours the mixture is filtered, the residue dissolved in water and the solution made basic with 12.5% aqueous sodium hydroxide. It is extracted with methylene chloride, dried and evaporated to yield the 1-benzyl-4-(2-phenylaminoethylamino)-piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04073911
Source datasetuspto-grants-1978_02
ORD IDord-51fab4380d884453bbe2cd08d6aa7266
Source noteuspto-grants-1978_02