Hydrochloric Acid → HCID 178444555, Verbindung
Reaktionsgleichung
[CH2:1]([C@H:6]1[CH2:11][CH2:10][C@H](C#N)[CH2:8][CH2:7]1)[CH2:2][CH2:3][CH:4]=[CH2:5].[OH-:14].[K+].Cl.C(O)CO[CH2:20][CH2:21][OH:22]>>[CH2:1]([C@H:6]1[CH2:11][CH2:10][C@H:20]([C:21]([OH:22])=[O:14])[CH2:8][CH2:7]1)[CH2:2][CH2:3][CH:4]=[CH2:5]Komponenten
Reaktionsbedingungen
- Temperatur
- 180 °C
Versuchsvorschrift
A solution of 2.9 g of trans-4-(4-pentenyl)cyclohexanecarbonitrile in 80 ml of diethylene glycol was treated with 8.0 g of potassium hydroxide and the mixture was stirred for 3.5 hours at a bath temperature of 180° C. Subsequently, the reaction mixture was treated with ice, made acid with 25 ml of 25 percent hydrochloric acid and partitioned in methylene chloride/water. The aqueous phase was extracted three times with methylene chloride. The organic phases were washed twice with water, dried over magnesium sulphate, filtered and concentrated. Chromatographic separation of the brown, oily residue (3.5 g) on silica gel with ethyl acetate/petroleum ether (vol. 10:90) gave 2.9 g (90%) of trans-4-(4-pentenyl)cyclohexanecarboxylic acid as a yellowish oil.
Aufarbeitung
- additionSubsequently, the reaction mixture was treated with ice
- custompartitioned in methylene chloride/water
- extractionThe aqueous phase was extracted three times with methylene chloride
- washThe organic phases were washed twice with water
- dry with materialdried over magnesium sulphate
- filtrationfiltered
- concentrationconcentrated
- customChromatographic separation of the brown, oily residue (3.5 g) on silica gel with ethyl acetate/petroleum ether (vol. 10:90)
Quellen und Nachweise
- ORD-Eintrag
- ord-f4d40b076efd488dabe3182071a25828
- Quelldatensatz
- uspto-grants-1993_08
- Patentnummer
- US05238602
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