Hydrochloric Acid → 2-(6-m-Methoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dione
Reaktionsgleichung
C(N(CC)[CH2:4][CH2:5][C:6](=[O:18])[CH2:7][CH2:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([O:16][CH3:17])[CH:11]=1)C.[CH3:21][CH:22]1[C:26](=[O:27])[CH2:25][CH2:24][C:23]1=[O:28].[Na].Cl>CO.[Cl-].[Na+].O.CCOCC>[CH3:17][O:16][C:12]1[CH:11]=[C:10]([CH2:9][CH2:8][CH2:7][C:6](=[O:18])[CH2:5][CH2:4][C:22]2([CH3:21])[C:26](=[O:27])[CH2:25][CH2:24][C:23]2=[O:28])[CH:15]=[CH:14][CH:13]=1Komponenten
8
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
Add the crude methiodide of 1-diethylamino-6-m-methoxyphenylhexan-3-one (2.5 g) in methanol (10 cc) ice-cold to a solution obtained by adding 2-methylcyclopentane-1,3-dione (0.5 g) to an ice-cold solution of sodium (0.21 g) in methanol (10 cc). Allow the reaction mixture to warm to room temperature and leave for 16 hours, after which add N hydrochloric acid (10 cc) and saturated brine (100 cc), and ether-extract the solution. Evaporate the washed and dried extracts to obtain the crude adduct 2-(6-m-methoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dione as a gum.
Aufarbeitung
- customobtained
- customleave for 16 hours
- extractionextract the solution
- customEvaporate the
- washwashed
- customdried extracts
Quellen und Nachweise
- ORD-Eintrag
- ord-542e4f692b414cf0888e64d38dd24de6
- Quelldatensatz
- uspto-grants-1977_01
- Patentnummer
- US04002746
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