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HRID 2073310作成日:2026年10月26日

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

https://huagongshe.com/reaction/2073310

反応式

関与物質

役割名称HCID仕込み量
反応物N-[1,1-dimethyl(3-pyridyl)butyl]-2-nitrobenzeneacetamideHCID 14347488—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒Acetic AcidHCID 176—
生成物alpha,alpha-Dimethyl-3-pyridinebutanamineHCID 1454728677.8%

反応手順

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 IL of water and extracted with ethyl acetate (4×200 mL) to remove the by product, 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,alphadimethyl-3-pyridinebutanamine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04916145
出典データセットuspto-grants-1990_04
ORD IDord-a8f5e68d62344dd7b2f30288b5e05637
出典メモuspto-grants-1990_04