Solid-liquid phase transfer catalytic synthesis VII: The synthesis of α-substituted-2-pyridylmethylamine via the alkylation of benzaldehyde imine

Article abstract of DOI:10.1080/00397919208021301

The anion derived from the benzaldehyde imine 2 reacts with alkyl halide to form alkylated products 3; Hydrolysis of 3 gives α-alkyl-2 pyridylmethylamine in 34-53% overall yield.

Full text of DOI:10.1080/00397919208021301

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Solid-Liquid Phase Transfer
Catalytic Synthesis. VII The
Synthesis of α-Substituted-2-
pyridylmethyl-amine via the
Alkylation of Benzaldehyde
Imine
Yuliang Wang a , Aiqiao Mi a & Yaozhong Jiang a
a Chengdu Institute of Organic Chemistry, Academia
Sinica , Chengdu, 610015, P. R. China
Published online: 23 Sep 2006.
To cite this article: Yuliang Wang , Aiqiao Mi & Yaozhong Jiang (1992) Solid-Liquid
Phase Transfer Catalytic Synthesis. VII The Synthesis of α-Substituted-2-pyridylmethyl-
amine via the Alkylation of Benzaldehyde Imine, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 22:2,
265-269, DOI: 10.1080/00397919208021301
To link to this article: http://dx.doi.org/10.1080/00397919208021301
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