Triethylamine → 1-[4-(Methylsulfonyl)phenyl]-3-methylpentane-1,4-dione

HRID 1597495

Reaktionsgleichung

Reaktionsgleichung von HRID 1597495
[CH3:1][S:2]([C:5]1[CH:12]=[CH:11][C:8]([CH:9]=[O:10])=[CH:7][CH:6]=1)(=[O:4])=[O:3].[CH3:13][C:14](=[CH2:18])[C:15](=[O:17])[CH3:16].CCN(CC)CC>C(O)C.[Cl-].C([N+]1C(C)=C(CCO)SC=1)C1C=CC=CC=1>[CH3:1][S:2]([C:5]1[CH:12]=[CH:11][C:8]([C:9](=[O:10])[CH2:13][CH:14]([CH3:18])[C:15](=[O:17])[CH3:16])=[CH:7][CH:6]=1)(=[O:3])=[O:4]

Komponenten

6

Edukt 3

HCID 8471TriethylamineHCID 13143Methyl isopropenyl ketoneHCID 2203764-(Methylsulfonyl)benzaldehyde

Produkt 1

HCID 218628391-[4-(Methylsulfonyl)phenyl]-3-methylpentane-1,4-dioneAusbeute 4,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 28333523-Benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chlorideKatalysatorHCID 702EthanolLösungsmittel

Versuchsvorschrift

To a stirred solution of 4-(methylsulfonyl)benzaldehyde (1.84 g, 10 mmol) in ethanol (8 mL) was added 3-methyl-3-buten-2-one (0.8 g, 9.5 mmol), 3-benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chloride (0.51 g, 1.9 mmol), and Et3N (2.65 mL, 19 mmol) at room temperature. After stirring for 3 hours, volatiles were removed by evaporation. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate/hexane (1/2) to provide the subtitle compound (0.11 g).

Aufarbeitung

  1. customvolatiles were removed by evaporation
  2. customThe residue was purified by flash chromatography on silica gel eluting with ethyl acetate/hexane (1/2)

Quellen und Nachweise

ORD-Eintrag
ord-35a3a8ebfa724cb1bea6a6654ca9acab
Quelldatensatz
uspto-grants-2001_09
Patentnummer
US06294558B1

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