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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651200Generated: October 25, 2026

N-[1,1-dimethyl(3-pyridyl)butyl]-2-nitrobenzeneacetamide → alpha,alpha-Dimethyl-3-pyridinebutanamine

https://huagongshe.com/reaction/1651200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[1,1-dimethyl(3-pyridyl)butyl]-2-nitrobenzeneacetamideHCID 14347488—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Productalpha,alpha-Dimethyl-3-pyridinebutanamineHCID 1454728677.8%

Reaction Steps

A solution of 35.2 g of N-[1,1-dimethyl-4-(3-pyridyl)butyl]-2-nitrobenzeneacetamide in 250 mL of acetic acid was hydrogenated over 3.5 g of 10% Pd/C at atmospheric pressure and ambient temperature. The reaction was exothermic and stopped abruptly after the uptake of the theoretical amount of hydrogen (7.5 L). The catalyst was removed by filtration and the filtrate was heated at reflux for 90 minutes. After the solution was cooled, 10 mL of conc. HCl was added and the solvent was removed under reduced pressure. The residue was taken up in 1 L of water and extracted with ethyl acetate (4×200 mL) to remove the byproduct, oxindole. The aqueous layer was basified with 10N NaOH and extracted with dichloromethane to give, after evaporation of the dried (K2CO3) extracts 15 g of product. The material was distilled on a Kugelrohr apparatus (95° C.; 0.1 mm) to yield 14.3 g of alpha,alpha-dimethyl-3-pyridinebutanamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04927838
Source datasetuspto-grants-1990_05
ORD IDord-4c0a2ba9e70c47b28bbffcd679e59c87
Source noteuspto-grants-1990_05