Reaktionsgleichung
[CH2:1]([C:3]([C:7]1[CH2:11][CH:10]=[CH:9][CH:8]=1)([CH3:6])[CH2:4][CH3:5])[CH3:2].[CH3:12][C:13]([CH3:15])=O.N1CCCC1>CO.CCOCC.O>[CH2:1]([C:3]([C:7]1[CH:11]=[CH:10][C:9](=[C:13]([CH3:15])[CH3:12])[CH:8]=1)([CH3:6])[CH2:4][CH3:5])[CH3:2]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
To a solution of 2.50 g (16.6 mmol) of (1-ethyl-1-methylpropyl)cyclopentadiene in 20 ml of methanol, 8.4 ml (114.4 mmol) of acetone and 2.8 ml (33.5 mmol) of pyrrolidine were added with ice cooling, followed by stirring at room temperature for one night. After the reaction solution was diluted with 100 ml of ether, 50 ml of water was added. The organic phase was separated, washed with water and a saturated saline solution, then dried over anhydrous 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 2.90 g (15.24 mmol) of a yellow liquid (yield: 92%). The analyzed values are given below.
Aufarbeitung
- additionwas added
- customThe organic phase was separated
- washwashed with water
- dry with materiala saturated saline solution, then dried over anhydrous 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-58d65a852bf5468993c9d656b84e0f6a
- Quelldatensatz
- uspto-grants-2008_11
- Patentnummer
- US07449533B2
Verknüpfte Notizen
Wird geladen…