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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22174Generated: October 26, 2026

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

https://huagongshe.com/reaction/22174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantMalonic AcidHCID 867—
ReactantTriethylamineHCID 8471—
Reactant4-Methoxy-1,3-dihydro-2-benzofuran-1,3-dioneHCID 291193—
SolventWaterHCID 962—
Product3-Hydroxy-7-methoxy-3-methyl-phthalideHCID 19927438—

Reaction Conditions

Temperature73 °C

Reaction Steps

5.4 g of 3-methoxy-phthalic acid anhydride [see A. V. R. Rao et al., Indian J. Chem. 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428002
Source datasetuspto-grants-1995_06
ORD IDord-321bce556ec0470c8cdb100a6ae37967
Source noteuspto-grants-1995_06