참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon Dioxide | HCID 280 | — |
| 반응물 | Malonic Acid | HCID 867 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Methoxy-1,3-dihydro-2-benzofuran-1,3-dione | HCID 291193 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 3-Hydroxy-7-methoxy-3-methyl-phthalide | HCID 19927438 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05428002 |
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| 출처 데이터셋 | uspto-grants-1995_06 |
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| ORD ID | ord-321bce556ec0470c8cdb100a6ae37967 |
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| 출처 메모 | uspto-grants-1995_06 |
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