Reaktionsgleichung
Br[C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH3:29][C:30]([CH3:34])([CH3:33])[C:31]#[CH:32]>C(N(CC)CC)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH3:29][C:30]([CH3:34])([CH3:33])[C:31]#[C:32][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1Komponenten
6
Versuchsvorschrift
A mixture of 4-bromobenzaldehyde (3.7 g), triphenylphosphine (0.32 g), palladium(II) acetate (135 mg), and 3,3-dimethyl-1-butyne (4 ml) in triethylamine (20 ml) is thoroughly purged with nitrogen, then heated to 100° in a sealed tube under nitrogen for 2 hr. The mixture is cooled, and the precipitated triethylamine hydrobromide is removed by filtration. The filtrate is concentrated, and the residue dissolved in 3:1 dichloromethane-hexane and filtered through a 2-cm pad of silica gel. The filtrate is concentrated and vacuum-distilled to provide 4-(3,3-dimethyl-1-butynyl)benzaldehyde as a pale yellow solid (3.25 g, 86%).
Aufarbeitung
- customis thoroughly purged with nitrogen
- temperatureheated to 100° in a sealed tube under nitrogen for 2 hr
- temperatureThe mixture is cooled
- customthe precipitated triethylamine hydrobromide is removed by filtration
- concentrationThe filtrate is concentrated
- dissolutionthe residue dissolved in 3:1 dichloromethane-hexane
- filtrationfiltered through a 2-cm pad of silica gel
- concentrationThe filtrate is concentrated
- distillationvacuum-distilled
Quellen und Nachweise
- ORD-Eintrag
- ord-36d789816f734a5da602139274dad03b
- Quelldatensatz
- uspto-grants-1995_11
- Patentnummer
- US05464865
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