Unknown

Dataset Information

0

4,5-Bis(4-fluoro-phen-yl)-5-hy-droxy-3-(2-methyl-propano-yl)-1-phenyl-pyrrolidin-2-one.


ABSTRACT: The title compound, C(26)H(23)F(2)NO(3), was synthesized by the reaction of 2-(4-fluoro-benzyl-idene)-4-methyl-3-oxo-N-phenyl-penta-namide and 4-fluoro-benzaldehyde. The dihedral angles between the mean plane through the pyrrolidine ring (nearly planar; maximum deviation of 0.145 Å for the C atom bearing the hydroxy group) with the phenyl and benzene rings are 37.22 (7), 51.88 (7) and 87.64 (9)°, respectively. The pyyolidine ring is near coplaner, with max offset of 0.145 A for C19 atom.\uff09 In the crystal, mol-ecules are linked by pairs of O-H⋯O hydrogen bonds into inversion dimers, which are further assembled into chains parallel to the b axis by weak C-H⋯O hydrogen bonds.

SUBMITTER: Huang JY 

PROVIDER: S-EPMC3099992 | biostudies-literature | 2011 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications

4,5-Bis(4-fluoro-phen-yl)-5-hy-droxy-3-(2-methyl-propano-yl)-1-phenyl-pyrrolidin-2-one.

Huang Jian-Ying JY   Zhou Fengyan F  

Acta crystallographica. Section E, Structure reports online 20110312 Pt 4


The title compound, C(26)H(23)F(2)NO(3), was synthesized by the reaction of 2-(4-fluoro-benzyl-idene)-4-methyl-3-oxo-N-phenyl-penta-namide and 4-fluoro-benzaldehyde. The dihedral angles between the mean plane through the pyrrolidine ring (nearly planar; maximum deviation of 0.145 Å for the C atom bearing the hydroxy group) with the phenyl and benzene rings are 37.22 (7), 51.88 (7) and 87.64 (9)°, respectively. The pyyolidine ring is near coplaner, with max offset of 0.145 A for C19 atom.\uff09 I  ...[more]

Similar Datasets

| S-EPMC9635426 | biostudies-literature
| S-EPMC3007318 | biostudies-literature
| S-EPMC3297871 | biostudies-literature
| S-EPMC3344118 | biostudies-literature
| S-EPMC3212291 | biostudies-literature
| S-EPMC3998389 | biostudies-literature
| S-EPMC3914103 | biostudies-literature
| S-EPMC3914111 | biostudies-literature
| S-EPMC3470376 | biostudies-literature
| S-EPMC4051101 | biostudies-literature