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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1729166Erstellt: 25. Oktober 2026

Carbon Dioxide → 3-Hydroxy-7-methoxy-3-methyl-phthalide

https://huagongshe.com/reaction/1729166

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
EduktMalonic AcidHCID 867—
EduktTriethylamineHCID 8471—
Edukt4-Methoxy-1,3-dihydro-2-benzofuran-1,3-dioneHCID 291193—
LösungsmittelWaterHCID 962—
Produkt3-Hydroxy-7-methoxy-3-methyl-phthalideHCID 19927438—

Reaktionsbedingungen

Temperatur73 °C

Reaktionsschritte

5.4 g of 3-methoxy-phthalic acid anhydride [see A. V. R. Rao et al., Indian J. Chew. 20B, 248 ff. (1981)], 4.7 g of malonic acid and 9 ml of triethylamine are heated slowly. The suspension becomes stirrable at 55° C. and, from 68° C., moderately vigorous CO2 evolution occurs. The internal temperature is maintained at 73° C. until gas evolution ceases (about 1 hour) and the reaction mixture is then heated at reflux temperature (internal temperature 85° C.) for a further 4 hours. When it has cooled, the reaction mixture is treated with water and extracted with ethyl acetate. The aqueous phase is then adjusted to pH 1.7 and extracted three times with fresh ethyl acetate, dried over anhydrous sodium sulfate and concentrated by evaporation under reduced pressure. Fractional crystallisation (ethyl acetate/n-hexane) yields 3-hydroxy-7-methoxy-3-methyl-phthalide, m.p. 156°-158° C.; IR spectrum (CHCl3): C=O 1772 cm-1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05332717
Quelldatensatzuspto-grants-1994_07
ORD IDord-ffe60877d1be4aec983195fadfb84c74
Quellennotizuspto-grants-1994_07