Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1322430 | Journal of Organometallic Chemistry | 2011 | 6 Pages |
A new synthesis leading to the chiral amidines (S,S)- and (R,R)-N,N-bis-(1-phenylethyl)benzamidine ((S)- and (R)-HPEBA) in good yields is presented. Further reaction of (S)-HPEBA with n-BuLi gave the chiral lithium salt (S)-LiPEBA. Treatment of KH with (S)-HPEBA in boiling THF afforded the corresponding potassium salt (S)-KPEBA. In contrast by performing the reaction in boiling toluene a fast racemization was observed. In the solid state racemic KPEBA formed a dimer, in which all four nitrogen atoms are in a plane. To each potassium atom a toluene molecule is η6-coordinated.
Graphical abstractA new synthesis leading to the chiral amidines (S,S)- and (R,R)-N,N-bis-(1-phenylethyl)benzamidine ((S)- and (R)-HPEBA) is presented. Further reaction of (S)-HPEBA to the chiral lithium (S)-LiPEBA and potassium salt (S)-KPEBA are described.Figure optionsDownload full-size imageDownload as PowerPoint slide