Lithium hydroxide, monohydrate → 2,3-Dihydro-6-methoxy-3-oxo-1H-indene-5-carboxylic acid
Reaktionsgleichung
C[O:2][C:3]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][C:13]=1[O:14][CH3:15])[CH2:10][CH2:9][C:8]2=[O:16])=[O:4].O[Li].O>C1COCC1.O>[CH3:15][O:14][C:13]1[CH:12]=[C:11]2[C:7]([C:8](=[O:16])[CH2:9][CH2:10]2)=[CH:6][C:5]=1[C:3]([OH:4])=[O:2]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
6-Methoxy-3-oxo-indan-5-carboxylic acid methyl ester (4 g, 18.18 mmol) was added to a solution of LiOH.H2O (2.2 g, 54.5 mmol) in THF (40 ml) and H2O (40 ml), then the mixture was heated to reflux and stirred for one hour. After removal of THF, the residue was acidified to PH=3, and the precipitate was collected and dried to give a white solid (3.38 g, 89.8%). LC-MS: m/e 207 (MH+)
Aufarbeitung
- temperaturethe mixture was heated
- temperatureto reflux
- customAfter removal of THF
- customthe precipitate was collected
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-5dd27c492fec41a382126e7032e88c80
- Quelldatensatz
- uspto-grants-2009_08
- Patentnummer
- US07572809B2
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