Aniline → 2,5-Bis(4-nitrophenyl)-1-phenylpyrrolidine

HRID 1470918

Reaktionsgleichung

Reaktionsgleichung von HRID 1470918
CS(O[CH:6]([C:24]1[CH:29]=[CH:28][C:27]([N+:30]([O-:32])=[O:31])=[CH:26][CH:25]=1)[CH2:7][CH2:8][CH:9](OS(C)(=O)=O)[C:10]1[CH:15]=[CH:14][C:13]([N+:16]([O-:18])=[O:17])=[CH:12][CH:11]=1)(=O)=O.[NH2:33][C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1>>[N+:16]([C:13]1[CH:14]=[CH:15][C:10]([CH:9]2[CH2:8][CH2:7][CH:6]([C:24]3[CH:29]=[CH:28][C:27]([N+:30]([O-:32])=[O:31])=[CH:26][CH:25]=3)[N:33]2[C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)=[CH:11][CH:12]=1)([O-:18])=[O:17]

Komponenten

3

Edukt 2

HCID 6115AnilineHCID 596171791,4-Bis(4-nitrophenyl)butane-1,4-diyl dimethanesulfonate

Produkt 1

HCID 866490982,5-Bis(4-nitrophenyl)-1-phenylpyrrolidine

Versuchsvorschrift

A mixture of the product from Example 1C (50 mg, 0.102 mmol) and aniline (0.2 ml, 2.19 mmol) were stirred at rt for 48 h. The mixture was partitioned between 1N aq. HCl and ethyl acetate, and the organic layer was dried over Na2SO4, filtered and concentrated in vacuo. The crude product was purified by column chromatography on silica gel using a solvent gradient of 0-50% ethyl acetate in hexanes. The title compound was obtained as a yellow solid (19 mg, 48%).

Aufarbeitung

  1. customThe mixture was partitioned between 1N aq. HCl and ethyl acetate
  2. dry with materialthe organic layer was dried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customThe crude product was purified by column chromatography on silica gel using a solvent gradient of 0-50% ethyl acetate in hexanes

Quellen und Nachweise

ORD-Eintrag
ord-29f52ae4afd74fc8823d6effc3a746ab
Quelldatensatz
uspto-grants-2015_04
Patentnummer
US09006387B2

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