Sodium Hydroxide → HCID 66918073, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[C:3]([CH:9]2[CH2:11][CH:10]2[C:12]([O:14]CC)=[O:13])=[N:4][CH:5]=[C:6]([Cl:8])[CH:7]=1.[OH-].[Na+]>C(O)C>[Cl:1][C:2]1[C:3]([CH:9]2[CH2:11][CH:10]2[C:12]([OH:14])=[O:13])=[N:4][CH:5]=[C:6]([Cl:8])[CH:7]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
1.65 g of ethyl 2-(3,5-dichloropyridin-2-yl)cyclopropanecarboxylate (0.00634 mol) are dissolved in 20 ml of ethanol, 9.5 ml of sodium hydroxide 1M are added to the reaction mixture which is refluxed for 4 hours and left at room temperature overnight. After concentration in vacuo, 30 ml of water are added to the reaction mixture which is extracted twice with ethyl acetate (20 ml). The aqueous phase is acidified with HCl 1M. The precipate which forms is filtered, air-dried to yield to 1.35 g of 2-(3,5-dichloropyridin-2-yl)cyclopropanecarboxylic acid (87%).
Aufarbeitung
- temperatureis refluxed for 4 hours
- concentrationAfter concentration in vacuo, 30 ml of water
- additionare added to the reaction mixture which
- extractionis extracted twice with ethyl acetate (20 ml)
- filtrationThe precipate which forms is filtered
- customair-dried
Quellen und Nachweise
- ORD-Eintrag
- ord-c6ef5c40c0354a42b7ca6bba3d5c12a0
- Quelldatensatz
- uspto-grants-2011_04
- Patentnummer
- US07932396B2
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