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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232718Generated: November 2, 2026

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

https://huagongshe.com/reaction/2232718

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 1L 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 numberUS04788206
Source datasetuspto-grants-1988_11
ORD IDord-5c695892ed6a422bb1bc692febaf1ae2
Source noteuspto-grants-1988_11