Reaktionsgleichung
[Li].[CH3:2][Si:3](Cl)([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.II.[F:19][C:20](F)=[CH2:21]>O1CCCC1>[F:19][C:20]([Si:3]([CH3:2])([C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)=[CH2:21]Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of lithium wire (2.08 g, 300 mmol) in dry tetrahydrofuran (150 ml) was added methyldiphenylsilyl chloride (15.8 ml, 75 mmol) and a catalytic amount of iodine. The reaction mixture was sonicated for 40 min and then stirred overnight at room temperature. The reaction mixture was cooled to −78° C. and 1,1-difluoroethylene (approx. 225 mmol) was passed through the mixture for 30 min. The mixture was stirred at −78° C. for 2 h and then warmed to room temperature. The reaction mixture was quenched with saturated ammonium chloride solution and extracted with cyclohexane (×2). The combined extracts were washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography (silica, 1 kg) eluting with hexane, followed by cyclohexane. The appropriate fractions were combined and concentrated to give Preparation 83 (7 g) as a colourless oil.
Aufarbeitung
- customThe reaction mixture was sonicated for 40 min
- temperatureThe reaction mixture was cooled to −78° C.
- stirringThe mixture was stirred at −78° C. for 2 h
- temperaturewarmed to room temperature
- customThe reaction mixture was quenched with saturated ammonium chloride solution
- extractionextracted with cyclohexane (×2)
- washThe combined extracts were washed with brine
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- customThe residue was purified by column chromatography (silica, 1 kg)
- washeluting with hexane
- concentrationconcentrated
- customto give
Quellen und Nachweise
- ORD-Eintrag
- ord-d422fcd4c1484092af78090657f5c3c1
- Quelldatensatz
- uspto-grants-2011_03
- Patentnummer
- US07902232B2
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