Engineering Laboratory of Organometallic, Molecular Materials and Environment (LIMOME), Faculty of Sciences, Sidi Mohammed Ben Abdellah University, Fez 30000, Morocco
Salaheddine Boukhssas
Engineering Laboratory of Organometallic, Molecular Materials and Environment (LIMOME), Faculty of Sciences, Sidi Mohammed Ben Abdellah University, Fez 30000, Morocco
Younas Aouine
Engineering Laboratory of Organometallic, Molecular Materials and Environment (LIMOME), Faculty of Sciences, Sidi Mohammed Ben Abdellah University, Fez 30000, Morocco
Anouar Alami
Engineering Laboratory of Organometallic, Molecular Materials and Environment (LIMOME), Faculty of Sciences, Sidi Mohammed Ben Abdellah University, Fez 30000, Morocco
Hassane Faraj
Engineering Laboratory of Organometallic, Molecular Materials and Environment (LIMOME), Faculty of Sciences, Sidi Mohammed Ben Abdellah University, Fez 30000, Morocco
Hafid Zouihri
Laboratory of Materials Chemistry and Biotechnology of Natural Products, Faculty of Sciences, Moulay Ismail University, Meknes 50050, Morocco
Brahim El Bali
Independent Scientist, Oujda 60000, Morocco
Mohammed Lachkar
Engineering Laboratory of Organometallic, Molecular Materials and Environment (LIMOME), Faculty of Sciences, Sidi Mohammed Ben Abdellah University, Fez 30000, Morocco
The title compound, 4,4-bis(hydroxymethyl)-2-phenyl-2-oxazoline 2, a well-known substance, was resynthesized in high yields through a conventional method. The structure of compound 2 was characterized for the first time by a single-crystal X-ray structure determination. The compound was further established through NMR spectroscopy (1D and 2D). In the molecular packing, two molecules of 4,4-bis(hydroxymethyl)-2-phenyl-2-oxazoline interact through H-Bonds to define “dimers” in which phenyl groups interact especially using π…π contact.
