3287-17-0Relevant academic research and scientific papers
Preparation of 2-aryl-2H-benzotriazoles by zinc-mediated reductive cyclization of o-nitrophenylazophenols in aqueous media without the use of organic solvents
Liu, Guo-Bin,Zhao, Hong-Yun,Yang, Hong-Jie,Gao, Xiang,Li, Miao-Kui,Thiemann, Thies
, p. 1637 - 1640 (2008/02/11)
Zinc powder-mediated reductive cyclization of o-nitrophenylazophenols in alkaline solution affords the corresponding 2-aryl-2H-benzotriazoles in high yields under mild reaction conditions. No organic solvents are used in the reaction and only minimal amounts in the work-up.
Preparation of 2-(2H-Benzotriazol-2-yl)phenols by the Reduction of 2-phenols with Thiourea S,S-Dioxide
Tanimoto, Shigeo,Kamano, Takayoshi
, p. 647 - 649 (2007/10/02)
The reduction of 2-phenols 1 with thiourea S,S-dioxide and sodium hydroxide in a mixture of isopropyl alcohol and water at reflux provides 2-(2H-benzotriazol-2-yl)phenols 3 in excellent yields.
High molecular weight piperidine derivatives as UV stabilizers
-
, (2008/06/13)
Substituted high molecular weight hindered spiropiperidine compounds and polymer compositions stabilized by these compounds. The spiropiperidine compounds are prepared by reacting hindered 4-piperidinone hydrochloride with an activated benzene, such as resorcinol, in an acid medium.
