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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1921915Erstellt: 26. Oktober 2026

Dimethyl Sulfate → Methyl 2-methoxy-3-methylbenzoate

https://huagongshe.com/reaction/1921915

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfateHCID 6497—
Edukt3-Methylsalicylic AcidHCID 6738—
EduktPotassium CarbonateHCID 11430—
LösungsmittelAcetoneHCID 180—
ProduktMethyl 2-methoxy-3-methylbenzoateHCID 13229229—

Reaktionsschritte

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%). 1H NMR (500 MHz, CDCl3, 25° C.) δ: 2.26 (s, 3H, CH3), 3.78 (s, 3H, OCH3), 3.85 (s, 3H, OCH3), 6.98 (t, J=7.5, 1H, ArH), 7.27 (d, J=7.5, 1H, ArH), 7.58 (d, J=7.5, 1H, ArH); 13C NMR (500 MHz, CDCl3, 25° C.) δ: 15.7, 51.8, 61.1, 123.2, 124.3, 128.8, 132.4, 134.8, 158.1, 166.6.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08173800B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-28af11f704094426a869ba0dc6830139
Quellennotizuspto-grants-2012_05