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STUDIES ON THE SYNTHESIS AND REACTIONWITH ALKOXIDES OF 3-OXO-1,2-BENZOISOTHIAZOLINE-2-ACETAMIDE1,1-DIOXIDES
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作者 Guo Feng ZHAO Hua Zbeng YANG(Institute of Elemento-Organic Chemistry Nankai University, Tianjin, 300071) 《Chinese Chemical Letters》 SCIE CAS CSCD 1996年第6期509-510,共2页
New 3 -oxo-benzoisothiazoline-2-acetamide 1, 1-dioxides (IIa-b) ware synthesizedand whose reaction with alkoxides was studied. The reaction results indicated that differentproducts were obtained owing to the different... New 3 -oxo-benzoisothiazoline-2-acetamide 1, 1-dioxides (IIa-b) ware synthesizedand whose reaction with alkoxides was studied. The reaction results indicated that differentproducts were obtained owing to the different time of reaction with alkoxides 展开更多
关键词 OXO OF REACTIONWITH AND ON THE STUDIES acetamide1 ALKOXIDES
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Transfer kinetics of phenol between aqueous phase and N,N-di(1-methyl-heptyl) acetamide in kerosene 被引量:2
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作者 Zhu-xian, Y. Hui-fang, D. +1 位作者 Qi-hong, Z. Zu-ming, Z. 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2000年第2期19-23,共5页
The transfer kinetics of phenol between aqueous phase and N,N di(methyl heptyl) acetaminde (N503) in kerosene has been studied using Lewis cell technique. The effects of the factors including the concentrations of p... The transfer kinetics of phenol between aqueous phase and N,N di(methyl heptyl) acetaminde (N503) in kerosene has been studied using Lewis cell technique. The effects of the factors including the concentrations of phenol in aqueous phase and organic phase, the concentration of N503 in organic phase, the acidity of aqueous phase, the stirring speed and the temperature on the rates of forward and backward extraction of phenol have been examined. The regularity of extraction rate has been obtained. According to experimental results, the rates of both forward and backward extraction of phenol might be controlled by diffusion process. The diffusion step of phenol from aqueous phase to interface for forward extraction and from interface to aqueous phase for backward extraction might be the rate controlling steps. 展开更多
关键词 PHENOL transfer kinetics N N di(1 methyl heptyl) acetamide CLC number: X703 Document code: A Introduction
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Synthesis of Agomelatine by One-pot Catalytic Hydrogenation and Acetylation with NiO
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作者 YU Zhijun CHENG Zhengzai +8 位作者 XIE Cong ZENG Sheng DENG Haiying LIU Panpan HU Hai LI Guangyao DING Ling Mario Gauthier LI Shiqian 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2019年第2期453-458,共6页
Nano-NiO and bulk NiO were prepared from Ni(AC)_2·4 H_2O by coordination precipitation using aqueous ammonia and by a solid state reaction, respectively. The nickel oxide particles were characterized by X-ray Dif... Nano-NiO and bulk NiO were prepared from Ni(AC)_2·4 H_2O by coordination precipitation using aqueous ammonia and by a solid state reaction, respectively. The nickel oxide particles were characterized by X-ray Diffraction(XRD) and scanning electron microscopy(SEM). The results indicate that nano-sized NiO has a crystal phase with a standard face-centered cubic lattice structure, with a mean particle diameter of about 10 nm. The evaluation of the activity of nickel oxide nanoparticles in the catalytic hydrogenation of 7-methoxy-1-naphthylacetonitrile was carried out. The results demonstrate the efficient synthesis of the title compound by a one-pot catalytic hydrogenation and acetylation with NiO. The NiO nanoparticles displayed superior catalytic activity in the synthesis of agomelatine in the one-pot reaction.The total yield of agomelatine is over 81.8% with a purity of 99.2%, as determined by HPLC. The structure of agomelatine was confirmed by IR, MS, and 1 H NMR analysis. 展开更多
关键词 NANO-NIO homogeneous precipitation method catalytic hydrogenation AGOMELATINE N-[2-(7-Methoxy-1-naphthyl)ethyl]acetamide 7-Methoxy-1-naphthylacetonitrile
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