Potassium Carbonate → Ethyl-4-(2-methoxy-3-methylphenyl)-4-methyl-2-oxopentanoate

HRID 1444532Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1444532
[CH3:1][O:2][C:3]1[C:8]([CH3:9])=[CH:7][CH:6]=[CH:5][C:4]=1[C:10](O)([CH3:12])[CH3:11].[CH2:14]([O:16][C:17](=[O:25])[C:18]([O:20][Si](C)(C)C)=[CH2:19])[CH3:15].[Sn](Cl)(Cl)(Cl)Cl.C(=O)([O-])[O-].[K+].[K+]>ClCCl>[CH2:14]([O:16][C:17](=[O:25])[C:18](=[O:19])[CH2:20][C:10]([C:4]1[CH:5]=[CH:6][CH:7]=[C:8]([CH3:9])[C:3]=1[O:2][CH3:1])([CH3:12])[CH3:11])[CH3:15]

Komponenten

6

Versuchsvorschrift

71.37 g (395.96 mmol) of 2-(2-methoxy-3-methylphenyl)-propan-2-ol and 149 g (791.92 mmol) of 2-trimethylsilanyloxyacrylic acid ethyl ester are introduced into 1.1 l of dichloromethane. At −78° C., 44.8 ml (379.91 mmol) of tin tetrachloride is added in drops, and the batch is then stirred for three hours at this low temperature. 1.4 l of semiconcentrated potassium carbonate solution is carefully added in drops, and the reaction mixture is thus brought to room temperature. The batch is filtered, and the filtrate is extracted three times with ethyl acetate. The combined organic extracts are washed with brine, dried on sodium sulfate, and the solvent is spun off. The residue is chromatographed several times on silica gel (mobile solvent ethyl acetate/hexane). 45.81 g (41.6%) of the desired compound is isolated.

Aufarbeitung

  1. customis thus brought to room temperature
  2. filtrationThe batch is filtered
  3. extractionthe filtrate is extracted three times with ethyl acetate
  4. washThe combined organic extracts are washed with brine
  5. customdried on sodium sulfate
  6. customThe residue is chromatographed several times on silica gel (mobile solvent ethyl acetate/hexane)

Quellen und Nachweise

ORD-Eintrag
ord-ea3f820ea9ec4d4bac5063e6db0c38bb
Quelldatensatz
uspto-grants-2010_02
Patentnummer
US07662821B2

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