Water → 6-(Biphenyl-4-yl)hexanol
Reaktionsgleichung
C[O:2][C:3](=O)[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[CH:11][CH:10]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>C1COCC1>[C:12]1([C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:11]=[CH:10][C:9]([CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][OH:2])=[CH:14][CH:13]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
6-(Biphenyl-4-yl)hexanoic acid methyl ester (0.67 g, 2.4 mmol) in THF (5 ml) was added dropwise to lithium aluminium hydride (0.2 g, 5.3 mmol) in THF cooled to 0° C. After stirring for 1 day at room temperature, water (1 ml) then 5M sodium hydroxide (1 ml) followed by water (2 ml) were added cautiously followed by stirring at room temperature for 2 hours. The precipitate was filtered off and filtrate was evaporated to give 6-(biphenyl-4-yl)hexanol as a solid (MS: M+ =254).
Aufarbeitung
- additionwere added cautiously
- stirringby stirring at room temperature for 2 hours
- filtrationThe precipitate was filtered off
- customfiltrate was evaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-3469efc0c0bd4d1ea64b690e5edfb6e0
- Quelldatensatz
- uspto-grants-1995_06
- Patentnummer
- US05428065
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