47460-66-2Relevant articles and documents
N-substituted carbamates syntheses with alkyl carbamates as carbonyl source over Ni-promoted Fe3O4 catalyst
Shang, Jianpeng,Guo, Xiaoguang,Shi, Feng,Ma, Yubo,Zhou, Feng,Deng, Youquan
, p. 328 - 336 (2011)
A series of catalysts of magnetic iron oxide containing Ni with different nickel content were prepared with co-precipitation method and tested in the syntheses of N-substituted carbamates from various amines and alkyl carbamates. Under the optimized reaction conditions, various N-substituted carbamates were successfully synthesized with 90-98% isolated yield. The catalyst could be recovered based on the magnetic property of the catalyst and reused for five runs without deactivation. The catalysts were characterized with X-ray photoelectron spectroscopy, X-ray diffraction, temperature-programmed reduction, temperature-programmed desorption, and Moessbauer spectroscopy analyses. The results showed that the catalytic activity may be derived from the delicate synergy between Ni and Fe species resulted in specific basic sites. Quasi in situ FT-IR and isotopic tracer revealed that the formation of substituted urea was the key step and the N-substituted carbamate was formed via further alcoholysis of the substituted urea.
Attempted Cycloaddition of N-Ethoxycarbonylmethyleneamine to N-Ethoxycarbonylazepine: Formation of 4,4'-Bis(ethoxycarbonylamino)diphenylmethane
Murphy, William S.,Raman, Krishna P.
, p. 447 - 448 (2007/10/02)
Three products were formed in the boron-trifluoride-catalysed reaction of N-ethoxycarbonylmethyleneamine with N-ethoxycarbonylazepine, N-ethoxycarbonylaniline (2), 4-(N-ethoxycarbonylaminomethyl)-N-ethoxycarbonylaniline (3), and 4,4'-bis-(N-ethoxycarbonylamino)diphenylmethane (4).Product (4) was independently synthesised.The mechanisms of formation of the products (2), (3), and (4) were established.
