Butane → Lithium (2-trimethylsiloxy-ethyl)-cyclopentadienide
Reaktionsgleichung
[CH3:1][Si:2]([CH3:12])([CH3:11])[O:3][CH2:4][CH2:5][C:6]1[CH2:10][CH:9]=[CH:8][CH:7]=1.C([Li:17])CCC.CCCCCC.CCCC>CCOCC>[CH3:11][Si:2]([CH3:1])([CH3:12])[O:3][CH2:4][CH2:5][C-:6]1[CH:10]=[CH:9][CH:8]=[CH:7]1.[Li+:17]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To 7.33 g of (2-trimethylsiloxy-ethyl)-cyclopentadiene in ether, 16 ml of a 2.5 M butyllithium solution in hexane (40 mmol) is added. The addition is realised at −78° C. The immediate formation of a white solid and butane evolution are observed. It is maintained reacting for 3 hours. Then it is dried; the resulting solid washed with hexane, leaving a powdery white solid. (6.19 g, 33 mmol, Yield: 82%).
Aufarbeitung
- additionThe addition
- customis realised at −78° C
- temperatureIt is maintained
- customThen it is dried
- washthe resulting solid washed with hexane
- customleaving a powdery white solid
Quellen und Nachweise
- ORD-Eintrag
- ord-ea8c12fb02ce482a91eeade7d48ee1e0
- Quelldatensatz
- uspto-grants-2007_05
- Patentnummer
- US07211538B2
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