61986-71-8Relevant academic research and scientific papers
Solvolytic reactivity of heptafluorobutyrates and trifluoroacetates
Denegri, Bernard,Kronja, Olga
experimental part, p. 5927 - 5933 (2009/12/26)
(Chemical Equation Presented) A series of X,Y-substituted benzhydryl heptafluorobutyrates (1-6-HFB) and trifluoroacetates (1-6-TFA) were subjected to solvolysis in various methanol/water, ethanol/water, and acetone/water mixtures at 25°C. The LFER equation log k = sf(Ef + N f) was used to derive the nucleofuge-specific parameters (N f and sf) for SN1-type reaction. In comparison with TFA, the HFB leaving group is a better nucleofuge for less than 0.5 unit of Nf. X,Y-Substituted benzhydryl trifluoroacetates solvolyze by way of SN1 reactions unless electron-withdrawing groups are attached to aromatic rings. In such cases the substrates solvolyze faster than predicted for the SN1 route because of the change in mechanism. X,Y-Substituted benzhydryl heptafluorobutyrates examined here (Ef ≥ -7.7) solvolyze according to the SN1 pathway. The almost parallel log k vs. Ef lines in various solvents for HFBs and TFAs, and the corresponding slope parameters (sf are in the range of 0.91 and 0.83), indicate early TS with moderately advanced charge separation. NBO charges of HFB and TFA anions and the affinities obtained, all calculated at the PCM-B3LYP/6-311+G(2d,p)//PCM-B3LYP/6-311+G(2d, p) level, revealed that the HFB anion slightly better delocalizes the developing negative charge than TFA, and that the affinity of the benzhydrylium ion is slightly larger toward TFA than toward the HFB anion, which is in accordance with the greater solvolytic reactivity of HFB.
A practical synthesis of para di- and mono-substituted benzhydrylamines from benzhydrol precursors
Laurent, Mathieu,Marchand-Brynaert, Jacqueline
, p. 667 - 672 (2007/10/03)
A series of para-substituted benzhydrylamines 6 were obtained by substitution of the corresponding benzhydrol precursors 1 with phenyl carbamate 2 under acidic conditions, followed by basic hydrolysis of the carbamate intermediates 3. One unsymmetrical intermediate 3i has been resolved by preparative chiral chromatography. Subsequent deprotection of the carbamate function led to the recovery of enantiomerically pure (+)- and (-)- 4-chlorobenzhydryl amines.
