479-27-6Relevant articles and documents
Preparation method of a plurality of (hetero) aromatic polyamines
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Paragraph 0018-0021; 0051-0052; 0054, (2021/09/15)
The invention relates to the field of organic functional new material chemicals, and discloses a novel process technology for preparing a plurality of (hetero) aromatic polyamines through corresponding (hetero) aromatic polyfunctional hydroxamic acids (hydroxamic acid) before (re-arrangement). These (hetero) aromatic polyamines are well-known dyes and pigment and pharmaceutical pesticide-related fields of very wide range of critical fine chemical materials.
Activated carbon supported bimetallic catalysts with combined catalytic effects for aromatic nitro compounds hydrogenation under mild conditions
Huang, Lei,Lv, Yang,Wu, Shengtao,Liu, Pingle,Xiong, Wei,Hao, Fang,Luo, He'an
, p. 76 - 85 (2019/04/01)
Non-noble nickel catalysts have been widely studied and tried in hydrogenation, however the problem of nickel particle sintering is more and more common in high-loaded nickel catalysts. A series of highly dispersed bimetallic Ni-M/AC (M = Cu, Co, Fe or Zn) catalysts were prepared by incipient wetness impregnation methods and applied in 1-nitronaphthalene hydrogenation to 1-naphthylamine under mild reaction conditions. The prepared catalysts were characterized by XRD, BET, H2-TPR, TEM, HRTEM, HAADF-STEM, XPS, ICP, FT-IR and H2 chemisorption. The results show that the introduction of the metal promoter inhibits the sintering of the nickel and enhances the reducibility of the catalysts, leading to higher ratio of effective Ni° on the surface of the support, especially for Ni-Zn/AC sample. Moreover, the results of XPS indicate that the electron donating effect of Cu promoter increases surface electronic density of Ni, as a result, the electron-rich Ni might be produced because of the interfacial electronic effect, which favors the desorption and further impedes the hydrogenation of N-naphthylhydroxylamine. Ni-Zn/AC-350 with smaller nickel particles, better dispersion and larger content of effective Ni° presents the best catalytic performance in 1-nitronaphthalene hydrogenation to 1-naphthylamine under mild reaction conditions, it gives 100% conversion of 1-nitronaphthalene and 96.82% selectivity to 1-naphthylamine under 0.6 MPa and 90℃ for 5 h. Additionally, superior performances are also obtained in hydrogenation reactions of nitrobenzene, chloronitrobenzene, 1,5-dinitronaphthalene and 1,8-dinitronaphthalene over Ni-Zn/AC catalysts. With good hydrogenation activity the catalyst shows, the application prospect in industrial production of aromatic amine from aromatic nitro compounds has been becoming more and more extension.
A Co2B Mediated NaBH4 Reduction Protocol Applicable to a Selection of Functional Groups in Organic Synthesis
Lundevall, Frida Johanne,Elumalai, Vijayaragavan,Drageset, Audun,Totland, Christian,Bj?rsvik, Hans-René
supporting information, p. 3416 - 3425 (2018/07/29)
A high-yielding and high-rate reduction method that operates with alkenes, alkynes, azides, nitriles, and nitroarenes was developed and optimized. The method makes use of sodium borohydride reduction of CoSO4 under release of hydrogen along with the formation of Co2B as a nanoparticle material. The produced Co2B activates the various functional groups for hydride reduction. The protocol was proven to operate with an assortment of functional groups to provide good to excellent yields. Furthermore, the reduction method was successfully adapted, implemented, and developed for a continuous flow approach using the multi-jet oscillating disk (MJOD) flow reactor platform at atmospheric pressure.