Acetone → Methyl 2-methoxy-5-methylbenzoate

HRID 725908

Reaktionsgleichung

Reaktionsgleichung von HRID 725908
[CH3:1][C:2]1[CH:10]=[C:6]([C:7]([OH:9])=O)[C:5]([OH:11])=[CH:4][CH:3]=1.[C:12](=O)([O-])[O-].[K+].[K+].CC(C)=O.S([O:27][CH3:28])(OC)(=O)=O>O>[CH3:12][O:11][C:5]1[CH:4]=[CH:3][C:2]([CH3:1])=[CH:10][C:6]=1[C:7]([O:27][CH3:28])=[O:9]

Komponenten

6

Edukt 4

HCID 180AcetoneHCID 6497Dimethyl Sulfate2×HCID 69735-Methylsalicylic acidHCID 11430Potassium Carbonate

Produkt 1

HCID 10241396Methyl 2-methoxy-5-methylbenzoateAusbeute 91,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

5.07 g (33.32×10-3 mol) of 5-methylsalicylic acid and 22.33 g (161.6×10-3 mol) of anhydrous potassium carbonate are introduced into a 250-cm3 two-necked flask. 175 cm3 of anhydrous acetone are added under an inert atmosphere. The reaction mixture is stirred, 7.25 cm3 (76.62×10-3 mol) of dimethyl sulfate are added with a syringe and the mixture is brought to reflux for 6 h. Hydrolysis of the dimethyl sulfate is performed by adding 5 cm3 of water. After filtration and evaporation of the solvent, the residue is taken up with dichloromethane, dried over MgSO4 and then evaporated to dryness. The crude product is purified by chromatography on a silica column (eluent : CH2Cl2) to give 5.47 g (30.36×10-3 mol) of the expected ester, equivalent to a 91% yield.

Aufarbeitung

  1. temperatureto reflux for 6 h
  2. filtrationAfter filtration and evaporation of the solvent
  3. dry with materialdried over MgSO4
  4. customevaporated to dryness
  5. customThe crude product is purified by chromatography on a silica column (eluent : CH2Cl2)

Quellen und Nachweise

ORD-Eintrag
ord-17066b7e77ee45c292106a42aa098d58
Quelldatensatz
uspto-grants-1998_01
Patentnummer
US05708020

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