1421699-01-5

Basic information

• Product Name: (S)-2-(anilinodiphenylmethyl)pyrrolidine
• Synonyms: (S)-2-(anilinodiphenylmethyl)pyrrolidine
• CAS NO: 1421699-01-5
• Molecular Weight: 328.457
• Mol File: 1421699-01-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-(anilinodiphenylmethyl)pyrrolidine(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-(anilinodiphenylmethyl)pyrrolidine(1421699-01-5)
• EPA Substance Registry System: (S)-2-(anilinodiphenylmethyl)pyrrolidine(1421699-01-5)

Safety Data

• Hazardous Substances Data: 1421699-01-5(Hazardous Substances Data)

Upstream product

• 1072028-48-8 1-[(2S)-1-benzylpyrrolidin-2-yl]-1,1-diphenylmethanamine 
• 113304-84-0 N-benzyl-(S)-proline methyl ester 
• 591-50-4 iodobenzene 
• 1072028-50-2 (S)-(pyrrolidin-2-yl)diphenylmethanamine 
• 118970-95-9 (S)-1-benzyl-2-(hydroxydiphenylmethyl)pyrrolidine 
• 1072028-47-7 ((S)-1-benzylpyrrolidin-2-yl)diphenylazidomethane 

Relevant articles and documents

Synthesis of chiral 2-(anilinophenylmethyl)pyrrolidines and 2-(anilinodiphenylmethyl)pyrrolidine and their application to enantioselective borane reduction of prochiral ketones as chiral catalysts

Chiral diamines, 2-(anilinophenylmethyl)pyrrolidines and 2-(anilinodiphenylmethyl)pyrrolidine, were prepared from N-(tert-butoxycarbonyl) pyrrolidine or (S)-proline as a starting material, respectively. These chiral diamines were efficient for the catalytic enantioselective borane reduction of acetophenone. Using (S)-2-(anilinodiphenylmethyl)pyrrolidine, chiral secondary alcohols were obtained from prochiral ketones with good to excellent enantiomeric excesses (up to 98% ee).