65249-04-9Relevant academic research and scientific papers
Potassium hydroxide catalyzed addition of arylamines to styrenes
Jaspers, Daniel,Doye, Sven
experimental part, p. 1444 - 1448 (2011/08/03)
Potassium hydroxide is a competent and cheap catalyst for the intermolecular addition of arylamines to styrenes. The reactions are performed in nontoxic dimethyl sulfoxide and can be used for the large-scale synthesis of β-phenylethylamines. Georg Thieme Verlag Stuttgart - New York.
A convenient synthesis of 1-alkyl-1-phenylhydrazines from N-aminophthalimide
Nara, Shigeru,Sakamoto, Takeshi,Miyazawa, Etsuko,Kikugawa, Yasuo
, p. 87 - 98 (2007/10/03)
N-Alkylaminophthalimides were synthesized by condensation of N-aminophthalimide with aldehydes, and subsequent reduction of the intermediate with pyridine-borane in acetic acid. N-Phenylation and removal of the phthalimide group gave 1-alkyl-1-phenylhydrazines in high yield.
β-phenylethylamines, indolines and isoquinolones via hydroamination of styrenes by microwave irradiation
Seijas,Vázquez-Tato,Martínez
, p. 875 - 877 (2007/10/03)
Microwave irradiation promotes hydroamination of styrenes. This method can be used as a direct way of producing different kinds of bioactive compounds: open chain compounds like β-phenylethylamines or cyclized products like indolines or isoquinolones.
A TRIFLUOROMETHANESULFONIC ACID-CATALYZED REACTION OF ARYLHYDRAZINES WITH BENZENE
Ohta, Toshiharu,Miyake, Shinji,Shudo, Koichi
, p. 5811 - 5814 (2007/10/02)
Arylhydrazines reacted with benzene in the presence of trifluoromethanesulfonic acid (TFSA) to give aminobiphenyls.This is a general method for the synthesis of aminobiphenyls.
