HCID 54197900, Verbindung → HCID 69827195, Verbindung
Reaktionsgleichung
[N:1]1[CH:6]=[CH:5][C:4]([C:7]([C@H:9]2[CH2:14][CH2:13][CH2:12][CH2:11][C@H:10]2[C:15]([OH:17])=[O:16])=[O:8])=[CH:3][CH:2]=1>[OH-].[Na+]>[N:1]1[CH:6]=[CH:5][C:4]([C:7]([C@@H:9]2[CH2:14][CH2:13][CH2:12][CH2:11][C@@H:10]2[C:15]([OH:17])=[O:16])=[O:8])=[CH:3][CH:2]=1Komponenten
3
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 20 °C
Versuchsvorschrift
Cis-2-(4-pyridylcarbonyl)cyclohexanecarboxylic acid was dissolved in 10% sodium hydroxide (300 mL) and stirred at 20° C. for 16 h. The aqueous solution was extracted with diethyl ether (200 mL) and then acidified to pH=4 by addition of 6 M hydrochloric acid. The resulting precipitate was collected and recrystallized from hot water, to give (1S, 2R)-2-(4-pyridylcarbonyl)cyclohexanecarboxylic acid, as a white solid (4.8 g, 40% from cis-1,2-cyclohexanedicarboxylic anhydride).
Aufarbeitung
- extractionThe aqueous solution was extracted with diethyl ether (200 mL)
- additionacidified to pH=4 by addition of 6 M hydrochloric acid
- customThe resulting precipitate was collected
- customrecrystallized from hot water
Quellen und Nachweise
- ORD-Eintrag
- ord-1b29e504a58a4419927d94ed5f1c07c8
- Quelldatensatz
- uspto-grants-2002_06
- Patentnummer
- US06410781B1
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