Pyrrolidine → E-1-(1-pyrrolidinyl)-2-[2-nitro-4-(4-fluorophenoxy)phenyl]ethylene

HRID 263437

Reaktionsgleichung

Reaktionsgleichung von HRID 263437
[N+:1]([C:4]1[CH:9]=[C:8]([O:10][C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)[CH:7]=[CH:6][C:5]=1[CH3:18])([O-:3])=[O:2].CO[CH:21](OC)[N:22]([CH3:24])[CH3:23].N1CC[CH2:29][CH2:28]1>CN(C)C=O>[N:22]1(/[CH:24]=[CH:18]/[C:5]2[CH:6]=[CH:7][C:8]([O:10][C:11]3[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=3)=[CH:9][C:4]=2[N+:1]([O-:3])=[O:2])[CH2:23][CH2:29][CH2:28][CH2:21]1

Komponenten

5

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

2-Nitro-4-(4-fluorophenoxy)toluene (11.8 g, 47.7 mmol), was dissolved in dimethylformamide (90.0 mL) under N2 atmosphere. Dimethylformamide dimethyl acetal (20.2 mL, 143 mmol), and pyrrolidine (4.0 mL, 47.4 mmol) were added via syringe and the reaction mixture was heated at 110° C. for 3 hours. The reaction mixture was cooled to ambient temperature and partitioned between H2O and ether. The organic phase was washed with H2O. The combined aqueous extracts were washed with ether. The ether extracts were combined and dried over Na2SO4, filtered, and concentrated in vacuo to give a viscous oil (16.1 g) which was used without further purification.

Aufarbeitung

  1. temperatureThe reaction mixture was cooled to ambient temperature
  2. custompartitioned between H2O and ether
  3. washThe organic phase was washed with H2O
  4. washThe combined aqueous extracts were washed with ether
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-91ad2b0cc9b648a99f036c8dce7d451b
Quelldatensatz
uspto-grants-1997_07
Patentnummer
US05643922

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