Water → 2-Fluoro-4-pentylbenzoic acid
Reaktionsgleichung
S(=O)(=O)(O)[OH:2].[OH2:6].[F:7][C:8]1[CH:15]=[C:14]([CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])[CH:13]=[CH:12][C:9]=1[C:10]#N>C(O)(=O)C>[F:7][C:8]1[CH:15]=[C:14]([CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])[CH:13]=[CH:12][C:9]=1[C:10]([OH:2])=[O:6]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of concentrated sulphuric acid (150 ml) and water (150 ml) was added dropwise to a stirred solution of compound 21 (15.0 g, 0.078 mol) in glacial acetic acid (300 ml). The stirred mixture was heated under reflux for 48 h, cooled in a refrigerator overnight and the product was filtered off. The product was dissolved in ether, extracted into 10% sodium hydroxide, which was then acidified with 36% hydrochloric acid, washed with ether (twice), and the combined ethereal phases were washed with water and dried (MgSO4). The solvent was removed in vacuo to give a brown crystalline solid.
Aufarbeitung
- temperatureThe stirred mixture was heated
- temperatureunder reflux for 48 h
- temperaturecooled in a refrigerator overnight
- filtrationthe product was filtered off
- dissolutionThe product was dissolved in ether
- extractionextracted into 10% sodium hydroxide, which
- washwashed with ether (twice), and the combined ethereal phases
- washwere washed with water
- dry with materialdried (MgSO4)
- customThe solvent was removed in vacuo
- customto give a brown crystalline solid
Quellen und Nachweise
- ORD-Eintrag
- ord-cb7d8e0d8b694f709bf72d5b6bacce8b
- Quelldatensatz
- uspto-grants-1992_10
- Patentnummer
- US05156763
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