591733-74-3Relevant articles and documents
Nucleophilic reactions at optically active bis(4-methyl-5-phenyl-1,3-oxazolidin-3-YL)methane
Salas-Coronado, Raul,Sanchez-Ruiz, Sonia A.,Galvez-Ruiz, Juan Carlos,Flores-Parra, Angelina
, p. 1111 - 1122 (2007/10/03)
The reagents RMgCl, RLi, NaOMe and amines (R = Me or t-Bu) with bis(4-methyl-5 -phenyl-1,3-oxazolidin-3-yl)methane (1) attack nucleophilically at its endo- or exocyclic methylenic groups (C-2 or C-6) giving: 3-ethyl-4-methyl-5phenyl-1,3-oxazolidine (3), 3-neopentyl-4-methyl-5-phenyl-1,3-oxazolidine (4), 2-[neopentyl-(4-methyl-5-phenylethan-1,3-oxazolidin-3-ylmethyl) amino]-1phenylpropan-1-ol (6), N-neopentyl norephedrine (7), 3-methoxymethyl-4methyl-5-phenyl-1,3-oxazolidine (8), N-benzyl-(4-methyl-5-phenyl-1,3oxazolidin-3-yl)methane (9), 2-chloropropyl-(4-methyl-5-phenyl-1,3-oxazolidin3-ylmethyl)amine (10), 2-[(benzylamino-methyl)amino]-1-phenylpropan-1-ol (11). A high yield synthesis of 3(H)-4-methyl-5-phenyl-1,3-oxazolidine (5) is also reported.