Ring-Opening Reactions of Nonactivated Aziridines Catalyzed by Tris(pentafluorophenyl)borane was written by Watson, Iain D. G.;Yudin, Andrei K.. And the article was included in Journal of Organic Chemistry in 2003.Name: Trans-2-(benzylamino)cyclohexanol This article mentions the following:
The ring-opening reactions of nonactivated aziridines with amine nucleophiles are efficiently catalyzed by tris(pentafluorophenyl)borane leading to the corresponding trans-1,2-diamines in high yields. A mechanistic investigation of the reaction suggests that in situ formed [(C6F5)3B(OH2)]·H2O catalyzes the opening through a Bronsted acid manifold. In the experiment, the researchers used many compounds, for example, Trans-2-(benzylamino)cyclohexanol (cas: 40571-86-6Name: Trans-2-(benzylamino)cyclohexanol).
Trans-2-(benzylamino)cyclohexanol (cas: 40571-86-6) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Name: Trans-2-(benzylamino)cyclohexanol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts