참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | ethyl 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylate | HCID 76918 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-Methylglutaconic anhydride | HCID 22086937 | — |
반응 단계
The procedure found in J. Am. Chem. Soc. 75, 2377-9 (1953) was generally followed. Ethyl isodehydroacetate (100 g, 0.51 mol) was added to a warm solution of sodium hydroxide (68.5 g., 0.71 mol) in water (500 mL) and stirred for an hour until the mixture became clear. The solution was acidified with concentrated hydrochloric acid (200 mL) and was extracted with ethyl acetate. The extract was dried over magnesium sulfate and concentrated by evaporation under reduced pressure. The residue was mixed with acetic anhydride (250 mL) and the resulting mixture was heated at reflux for 20-30 min. The solvent was removed by evaporation under reduced pressure and the residue obtained was crystallized from ether to obtain 60.8 g (94 percent of theory) of the title compound as a tan powder melting at 70°-72° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05571775 |
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| 출처 데이터셋 | uspto-grants-1996_11 |
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| ORD ID | ord-462a1656399e4ca7aab95d460877f575 |
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| 출처 메모 | uspto-grants-1996_11 |
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