Aluminium lithium hydride → (4-Phenyl-1,3-thiazol-2-yl)methanol
Reaktionsgleichung
[C:1]1([C:7]2[N:8]=[C:9]([C:12](OCC)=[O:13])[S:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[C:1]1([C:7]2[N:8]=[C:9]([CH2:12][OH:13])[S:10][CH:11]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To ethyl 4-phenylthiazole-2-carboxylate (1 g, 4.3 mmol) in anhydrous THF was added LiAlH4 and the mixture was stirred for 1 hour. The reaction was quenched with water, extracted with EtOAc and dried over anhydrous sodium sulfate. The solution was concentrated under vacuum to afford (4-phenylthiazol-2-yl)methanol as a white solid (0.9 g). MS (ESI) m/z 191 (M+H+).
Aufarbeitung
- customThe reaction was quenched with water
- extractionextracted with EtOAc
- dry with materialdried over anhydrous sodium sulfate
- concentrationThe solution was concentrated under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-2e11ec2db35248658c21fc491d8be895
- Quelldatensatz
- uspto-grants-2015_03
- Patentnummer
- US08969349B2
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