Morpholine → 4-(2-Fluoro-5-vinyl-phenyl)-morpholine

HRID 1825041Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1825041
Br[C:2]1[CH:7]=[C:6]([CH:8]=[CH2:9])[CH:5]=[CH:4][C:3]=1[F:10].[NH:11]1[CH2:16][CH2:15][O:14][CH2:13][CH2:12]1.[O-]P([O-])([O-])=O.[K+].[K+].[K+]>COCCOC.C(Cl)Cl.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[F:10][C:3]1[CH:4]=[CH:5][C:6]([CH:8]=[CH2:9])=[CH:7][C:2]=1[N:11]1[CH2:16][CH2:15][O:14][CH2:13][CH2:12]1

Komponenten

7

Versuchsvorschrift

A mixture of 2-Bromo-1-fluoro-4-vinyl-benzene (8 g), morpholine (20 mL), Pd2(dba)3 (1.83 g), di-t-butyl-biphenylphosphine (1.2 g), K3PO4 (17 g) in DME (60 mL) was stirred at reflux for 4 h. The reaction mixture was cooled down to room temperature, diluted with methylene chloride, and filtered. The filtrate was concentrated in vacuo. The crude product was purified by Flash Chromatography of Biotage eluting with 7% ethyl acetate in hexanes to give the title compound as an oil (5 g).

Aufarbeitung

  1. temperatureat reflux for 4 h
  2. filtrationfiltered
  3. concentrationThe filtrate was concentrated in vacuo
  4. customThe crude product was purified by Flash Chromatography of Biotage
  5. washeluting with 7% ethyl acetate in hexanes

Quellen und Nachweise

ORD-Eintrag
ord-f61ac025c53b4deeaacb1812444d7bf4
Quelldatensatz
uspto-grants-2006_05
Patentnummer
US07045551B2

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