Cyclohexylfulvene → (1-Methyl-1-cyclohexyl)cyclopentadiene
Reaktionsgleichung
[CH:1]1([C:7]2[C:11](=C)[CH:10]=[CH:9][CH:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:13][Li]>C1COCC1.CCOCC.O>[CH3:13][C:1]1([C:7]2[CH2:11][CH:10]=[CH:9][CH:8]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1Komponenten
Versuchsvorschrift
To a solution of 6.50 g (44.5 mmol) of cyclohexylfulvene in 60 ml of THF, 44.8 ml (51.1 mmol) of an ether solution of methyllithium was dropwise added in a nitrogen atmosphere with ice cooling, followed by stirring at room temperature for one night. After the reaction solution was diluted with 100 ml of ether, 30 ml of water was added. The separated organic phase was washed with water and a saturated saline solution, then dried over magnesium sulfate and filtered. From the filtrate, the solvent was removed under reduced pressure to obtain a liquid. The liquid was isolated and purified by column chromatography (silica gel, developing solvent: hexane) to obtain 2.72 g (16.76 mmol) of a colorless transparent liquid (yield: 38%) The analyzed values are given below.
Aufarbeitung
- additionwas added
- washThe separated organic phase was washed with water
- dry with materiala saturated saline solution, then dried over magnesium sulfate
- filtrationfiltered
- customFrom the filtrate, the solvent was removed under reduced pressure
- customto obtain a liquid
- customThe liquid was isolated
- custompurified by column chromatography (silica gel, developing solvent: hexane)
Quellen und Nachweise
- ORD-Eintrag
- ord-f30bcdc8296743108352e821da840924
- Quelldatensatz
- uspto-grants-2008_11
- Patentnummer
- US07449533B2
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