An article Lewis Acid-Catalyzed Nucleophilic Substitutions of Benzylic Alcohols with Sulfamides WOS:000596630100001 published article about PI-ACTIVATED ALCOHOLS; ALLYLIC ALCOHOLS; UNSYMMETRICAL SULFAMIDES; EFFICIENT SYNTHESIS; CHIRAL-AUXILIARY; DIRECT AMINATION; ASYMMETRIC ARYLATION; ALKYLATION REACTION; CONJUGATE ADDITION; SULFONAMIDES in [Oda, Ryoga; Nakata, Kenya] Shimane Univ, Dept Chem, Grad Sch Nat Sci & Technol, 1060 Nishikawatsu, Matsue, Shimane 6908504, Japan in 2021.0, Cited 104.0. The Name is Diphenylmethanamine. Through research, I have a further understanding and discovery of 91-00-9. Quality Control of Diphenylmethanamine
Nucleophilic substitutions of benzylic alcohols with sulfamides were achieved using an FeCl3 Lewis acid catalyst in MeNO2. It was necessary to adjust the reaction conditions to obtain efficient yields depending on the stability of the carbocation intermediates. The reaction could easily be performed, and it was revealed that a variety of diarylmethanols and benzylic alcohols were applicable to the reaction, irrespective of the type and position of the substituents. The sulfamide moieties were easily deprotected and converted into amine groups.
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Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics