7335-06-0Relevant articles and documents
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v. Braun
, p. 1256 (1911)
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Highly economical and direct amination of sp3carbon using low-cost nickel pincer catalyst
Brandt, Andrew,Rangumagar, Ambar B.,Szwedo, Peter,Wayland, Hunter A.,Parnell, Charlette M.,Munshi, Pradip,Ghosh, Anindya
, p. 1862 - 1874 (2021/01/20)
Developing more efficient routes to achieve C-N bond coupling is of great importance to industries ranging from products in pharmaceuticals and fertilizers to biomedical technologies and next-generation electroactive materials. Over the past decade, improvements in catalyst design have moved synthesis away from expensive metals to newer inexpensive C-N cross-coupling approaches via direct amine alkylation. For the first time, we report the use of an amide-based nickel pincer catalyst (1) for direct alkylation of amines via activation of sp3 C-H bonds. The reaction was accomplished using a 0.2 mol% catalyst and no additional activating agents other than the base. Upon optimization, it was determined that the ideal reaction conditions involved solvent dimethyl sulfoxide at 110 °C for 3 h. The catalyst demonstrated excellent reactivity in the formation of various imines, intramolecularly cyclized amines, and substituted amines with a turnover number (TON) as high as 183. Depending on the base used for the reaction and the starting amines, the catalyst demonstrated high selectivity towards the product formation. The exploration into the mechanism and kinetics of the reaction pathway suggested the C-H activation as the rate-limiting step, with the reaction second-order overall, holding first-order behavior towards the catalyst and toluene substrate.
Method for catalytically synthesizing 1-substituted pyrrolidine/piperidine derivative by using supported metal
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Paragraph 0016, (2020/02/20)
The invention provides a method for catalytically synthesizing a 1-substituted pyrrolidine/piperidine derivative by using a supported metal. The method comprises: carrying out a reaction with ammoniato form a pyrrolidine ring/piperidine ring by using a supported metal as a catalyst, using 1,4-butanediol/1, 5-pentanediol as a cyclization raw material and using alcohol as an N-alkylation raw material, wherein the high-selectivity synthesis of the 1-substituted pyrrolidine/piperidine derivative is achieved through the one-step reaction, the active components of the supported metal catalyst are Cu, Ni and Pd/Ru, the total loading capacity of the active components Cu and Ni is 3-15 wt% of the carrier, and the loading capacity of Pd/Ru is 0-1 wt% of the carrier. According to the invention, themethod is simple, low in cost and environmentally friendly, the conversion rate of 1,4-butanediol/1,5-pentanediol is high, the selectivity of the pyrrolidine/piperidine derivatives is high, and the method is a production route with practical application value.
