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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 280721Erstellt: 23. Oktober 2026

Dimethyl Sulfate → Dimethyl Sulfate

https://huagongshe.com/de/reaction/280721

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfateHCID 6497—
Edukt2-Furancarboxylic acidHCID 6919—
EduktAnisoleHCID 7519—
EduktPotassium CarbonateHCID 11430—
LösungsmittelAcetoneHCID 180—
LösungsmittelPotassium HydroxideHCID 14797—
LösungsmittelSodiumHCID 5360545—
ProduktDimethyl SulfateHCID 6497—
Produkt2-Hydroxy-1-naphthoic acidHCID 16790—
ProduktMethyl 2-methoxy-1-naphthoateHCID 604022—

Reaktionsschritte

This methyl ester was previously made by fusion of anisole and 2-furoic acid followed by esterification of the acid intermediate, J. Amer. Chem. Soc., Vol. 69, 2261 (1947). Methyl esters of methoxy carboxylic acids were prepared by methylation of aromatic hydroxy carboxylic acids with dimethyl sulfate in the presence of potassium carbonate as base, using acetone as the solvent, Houben-Weyl, Methoden der Organischen Chemie., Vol. 8, 542-3 (1952). Methylation of 2-hydroxy-1-naphthoic acid with dimethyl sulfate in aqueous sodium or potassium hydroxide produced mainly methyl-2-methoxy-1-naphthalenecarboxylate, Chemische Berichte, Vol. 37, 3658-61 (1904). In aqueous solutions, at pH 4-6.5, methylation of hydroxy napthoic acids with dimethyl sulfate produced the methyl esters of the hydroxy naphthoic acids.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04590290
Quelldatensatzuspto-grants-1986_05
ORD IDord-c324ab068a684be1923eb42b45f5f752
Quellennotizuspto-grants-1986_05