Dimethyl Sulfate → Methyl 2-methoxy-3-methylbenzoate

HRID 1026527

Reaktionsgleichung

Reaktionsgleichung von HRID 1026527
[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:4]([C:5]([OH:7])=O)[C:3]=1[OH:11].[C:12](=O)([O-])[O-].[K+].[K+].COS([O:23][CH3:24])(=O)=O>CC(C)=O>[CH3:12][O:11][C:3]1[C:2]([CH3:1])=[CH:10][CH:9]=[CH:8][C:4]=1[C:5]([O:23][CH3:24])=[O:7]

Komponenten

5

Edukt 3

HCID 6497Dimethyl Sulfate2×HCID 67383-Methylsalicylic AcidHCID 11430Potassium Carbonate2×

Produkt 1

HCID 13229229Methyl 2-methoxy-3-methylbenzoate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 180AcetoneLösungsmittel

Versuchsvorschrift

To a mixture of 3-methyl-salicylic acid (200 g, 1.32 mol), anhydrous potassium carbonate (500 gram, 3.6 mol) and dry acetone (3.5 L) in a 5 liter round bottle flask, dimethylsulfate (DMS, 210 mL, 2.2 mol) was added in several portions. After stirring at room temperature overnight, the mixture was heated at reflux, and the reaction was monitored by TLC. In order to complete the etherification, further additions of DMS and K2CO3 may be necessary. When TLC indicated the completion of the reaction, the mixture was refluxed 4 more hours to destroy any remaining DMS. The mixture was filtered, and the filtrate was evaporated to remove the solvents. A pale yellow thick oil was obtained as the raw product, yield 215 g (91%).

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureat reflux
  3. customthe completion of the reaction
  4. temperaturethe mixture was refluxed 4 more hours
  5. customto destroy any remaining DMS
  6. filtrationThe mixture was filtered
  7. customthe filtrate was evaporated
  8. customto remove the solvents

Quellen und Nachweise

ORD-Eintrag
ord-8733cd2d05b0428ca65565aafccb6f50
Quelldatensatz
uspto-grants-2014_05
Patentnummer
US08729258B2

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