Sodium Carbonate → (E)-3-[4-(3-Pyridinyl)phenyl]-2-propenal
Reaktionsgleichung
C([O-])([O-])=O.[Na+].[Na+].[N:7]1[CH:12]=[CH:11][CH:10]=[C:9](B(O)O)[CH:8]=1.Br[C:17]1[CH:26]=[CH:25][C:20]([CH:21]=[CH:22][CH:23]=[O:24])=[CH:19][CH:18]=1>CO.C1(C)C=CC=CC=1.ClCCl.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[N:7]1[CH:12]=[CH:11][CH:10]=[C:9]([C:17]2[CH:26]=[CH:25][C:20](/[CH:21]=[CH:22]/[CH:23]=[O:24])=[CH:19][CH:18]=2)[CH:8]=1Komponenten
8
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 4
Versuchsvorschrift
2M aq. Na2CO3 (1 mL) and a solution of 3-pyridinylboronic acid (148 mg, 1.20 mmol) in methanol (1 mL) were added to a solution of 4-bromocinnamaldehyde (211 mg, 1.00 mmol, prepared as described in Tetrahedron 1998, 54, 10761) and tetrakis(triphenylphosphine)palladium(0) (35 mg, 0.030 mmol) in toluene (2 mL) and the mixture was heated to reflux for 36 h. The cooled reaction mixture was diluted with dichloromethane, washed with sat. aq. NaHCO3 and brine, dried (MgSO4), and concentrated. Purification by chromatography (SiO2, 1:1 hexane/ethyl acetate) yielded the title compound. MS 210 (M+H)+.
Aufarbeitung
- temperaturethe mixture was heated
- temperatureto reflux for 36 h
- customThe cooled reaction mixture
- washwashed with sat. aq. NaHCO3 and brine
- dry with materialdried (MgSO4)
- concentrationconcentrated
- customPurification by chromatography (SiO2, 1:1 hexane/ethyl acetate)
Quellen und Nachweise
- ORD-Eintrag
- ord-0cae008b30744e4cbe2ca6e2d7249d98
- Quelldatensatz
- uspto-grants-2004_03
- Patentnummer
- US06713455B2
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