Reaction of organozinc halides with aryl isocyanates
作者:Haoran Yang、Danfeng Huang、Ke-Hu Wang、Changming Xu、Teng Niu、Yulai Hu
DOI:10.1016/j.tet.2013.01.053
日期:2013.3
Reformatsky reagent, benzylzinc bromide or alkylzinc iodides react with arylisocyanates directly to give corresponding N-substituted carbamates under mild reaction conditions. However, the reaction of allylzinc bromide or propargylzinc bromide with arylisocyanates produces the corresponding N-substituted amides. The reactions provide alternative methods for the synthesis of N-substituted carbamates
METHOD FOR TREATMENT OF ISOCYANATE RESIDUE, AND METHOD FOR TREATMENT OF CARBONATE
申请人:Mitsui Chemicals, Inc.
公开号:EP2518044A1
公开(公告)日:2012-10-31
A method for treating an isocyanate residue, which comprises carrying out a thermal decomposition reaction of a carbamate that is produced by the reaction among an amine, urea and/or an N-unsubstituted carbamic acid ester and an alcohol to produce a decomposition solution, separating an isocyanate and the alcohol from the decomposition solution to produce the isocyanate residue, and bringing the isocyanate residue into contact with high-pressure/high-temperature water to decompose the isocyanate residue into an amine; and a method for treating a carbonate, which comprises bringing the carbonate into contact with high-pressure/high-temperature water to decompose the carbonate into an alcohol.