Valeryl chloride → 1-Heptyn-3-one, 1-(trimethylsilyl)-
Reaktionsgleichung
[C:1](Cl)(=[O:6])[CH2:2][CH2:3][CH2:4][CH3:5].[CH3:8][Si:9]([C:12]#[C:13][Si](C)(C)C)([CH3:11])[CH3:10].[Cl-].[Al+3].[Cl-].[Cl-]>C(Cl)Cl>[CH3:8][Si:9]([C:12]#[C:13][C:1]([CH2:2][CH2:3][CH2:4][CH3:5])=[O:6])([CH3:11])[CH3:10]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a stirred solution of 14.4 g of valeryl chloride and 20.4 g of bis-trimethylsilylacetylene in 300 ml of dry methylene chloride, cooled in an ice bath, is added powdered anhydrous aluminum chloride, portionwise, over a period of 20 minutes. The mixture is stirred for 5 minutes, then the cooling bath is removed and the mixture is stirred at room temperature for 4 hours. The mixture is poured into 500 ml of ice-water. The organic layer is separated, washed with water and brine, dried over anhydrous sodium sulfate and filtered through diatomaceous earth. The mother liquor is evaporated to dryness giving a brownish residue. This residue is Kugelrohr-distilled to give 16.56 g of colorless liquid at 45° C./0.3 mm which is essentially identical with the authentic product.
Aufarbeitung
- additionis added
- customthe cooling bath is removed
- stirringthe mixture is stirred at room temperature for 4 hours
- additionThe mixture is poured into 500 ml of ice-water
- customThe organic layer is separated
- washwashed with water and brine
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered through diatomaceous earth
- customThe mother liquor is evaporated to dryness
- customgiving a brownish residue
- distillationThis residue is Kugelrohr-distilled
Quellen und Nachweise
- ORD-Eintrag
- ord-74b42331a11245078ff99d4880a6e33e
- Quelldatensatz
- uspto-grants-1981_03
- Patentnummer
- US04254285
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