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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378931Generated: November 3, 2026

1-Benzyl-4-piperidylamine → N-(2-nitrophenethyl)-1-benzylpiperidin-4-amine

https://huagongshe.com/reaction/2378931

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-piperidylamineHCID 415852—
Reactant2-Nitrophenethyl bromideHCID 12363878—
ProductN-(2-nitrophenethyl)-1-benzylpiperidin-4-amineHCID 1620248781%

Reaction Conditions

Temperature100 °C

Reaction Steps

1-(2-Bromoethyl)-2-nitrobenzene (1.5 g, 6.52 mmol) and 4-amino-1-benzylpiperidine (3.0 ml, 14.71 mmol) were combined. Mixture was heated neat at 100° C. and held with stirring for 17 hours. Mixture was cooled to room temperature. Residue was triturated in 30 mL diethyl ether. Solids were filtered off, washed with diethyl ether and discarded. Filtrate was concentrated. Silica gel chromatography on the residue eluting 2M ammonia in methanol-dichloromethane afforded the title compound as brown oil in 81% yield. MS (M+H)+=340.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470680B2
Source datasetuspto-grants-2008_12
ORD IDord-2bb46510d6104a88951902a499dc8a15
Source noteuspto-grants-2008_12