Water → Meptazinol
Reaktionsgleichung
[CH2:1]([C:3]1([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([OH:18])[CH:13]=2)[CH2:9][CH2:8][CH2:7][CH2:6][N:5]([CH3:10])[C:4]1=O)[CH3:2].[H-].[Li+].[Al+3].[H-].[H-].[H-].O>O1CCCC1>[CH2:1]([C:3]1([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([OH:18])[CH:13]=2)[CH2:9][CH2:8][CH2:7][CH2:6][N:5]([CH3:10])[CH2:4]1)[CH3:2]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 3-ethylhexahydro-3-(3-hydroxyphenyl)-1-methyl-2H-azepin-2-one (1.5 g) in dry tetrahydrofuran was added to a stirred suspension of aluminium lithium hydride (0.48 g) and heated under reflux for 5 hours. The reaction mixture was cooled and decomposed by the addition of water and the precipitate filtered. The precipitate was washed with tetrahydrofuran and the combined filtrate and washings evaporated to a solid. The solid was dissolved in water and ammonium chloride added. The precipitated oil was extracted with dichloromethane, dried over anhydrous magnesium sulphate and evaporated to leave a solid which was recrystallised from acetonitrile to give 0.91 g of the title compound, m.p. 127.5°-133° C., identical with material prepared by an alternative route described in U.K. specification No. 1,285,025.
Aufarbeitung
- temperatureheated
- temperatureunder reflux for 5 hours
- temperatureThe reaction mixture was cooled
- filtrationthe precipitate filtered
- washThe precipitate was washed with tetrahydrofuran
- customthe combined filtrate and washings evaporated to a solid
- dissolutionThe solid was dissolved in water
- additionammonium chloride added
- extractionThe precipitated oil was extracted with dichloromethane
- dry with materialdried over anhydrous magnesium sulphate
- customevaporated
- customto leave a solid which
- customwas recrystallised from acetonitrile
Quellen und Nachweise
- ORD-Eintrag
- ord-addc622addb74b33917f9d6268941acb
- Quelldatensatz
- uspto-grants-1980_04
- Patentnummer
- US04197241
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