Efficient synthesis of methyl carbamate via Hofmann rearrangement in the presence of TsNBr 2
AJ Borah, P Phukan
Index: Borah, Arun Jyoti; Phukan, Prodeep Tetrahedron Letters, 2012 , vol. 53, # 24 p. 3035 - 3037
Full Text: HTML
Citation Number: 14
Abstract
An efficient method has been developed for the synthesis of carbamates from the corresponding amides via the Hofmann rearrangement using N, N-dibromo-p- toluenesulfonamide (TsNBr2) in the presence of DBU in methanol. The reaction goes into completion in 10–20min at 65° C to produce the corresponding carbamate in excellent yield.
Related Articles:
[Valli, V. L. K.; Alper, Howard Journal of the American Chemical Society, 1993 , vol. 115, # 9 p. 3778 - 3779]
[Alper, Howard; Hartstock, Frederick W. Journal of the Chemical Society, Chemical Communications, 1985 , # 16 p. 1141 - 1142]
[Alper, Howard; Hashem, Khaled E. Journal of the American Chemical Society, 1981 , vol. 103, # 21 p. 6514 - 6515]
[Alper, Howard; Hashem, Khaled E. Journal of the American Chemical Society, 1981 , vol. 103, # 21 p. 6514 - 6515]
[Guo, Xiaoguanga; Shang, Jianpenga; Li, Jiana; Wang, Liguoa; Ma, Yuboa; Shi, Feng; Deng, Youquan Chinese Journal of Chemistry, 2010 , vol. 28, # 2 p. 164 - 170]