참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Nitroethane | HCID 6587 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Phosphorus oxychloride | HCID 24813 | — |
| 반응물 | Ethyl 3-pyrrolidinocrotonate | HCID 736204 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | Ethyl 3,5-dimethylisoxazole-4-carboxylate | HCID 736348 | — |
반응 단계
A solution of the ethyl β-pyrrolidinocrotonate (427 g. = 2.33 moles), 190 ml. (182 g., 2.43 mole) of nitroethane and 1300 ml. of triethylamine in 1200 ml. of anhydrous chloroform was cooled in an ice bath under nitrogen. A solution of 235 ml. (393 g. = 2.56 mole) of phosphorous oxychloride in 400 ml. of chloroform was added at such a rate that the temperature did not rise above 15°. During the addition, which took place over a three-hour period, a viscous orange precipitate formed. This suspension was then stirred under nitrogen overnight. As much solvent as possible was removed at reduced pressure and the resulting red-brown paste was diluted with water and extracted with ether. The ether solutions were washed sequentially with water, 3N hydrochloric acid, water, 5 percent sodium hydroxide solution and water, and were dried over anhydrous sodium sulfate. Solvent removal at reduced pressure gave a dark oil which was distilled through a short Vigreux column to give 4-carboethoxy-3,5-dimethyl-isoxazole as a slightly cloudy, colorless liquid of b.p. 100° /11mm.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US03985771 |
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| 출처 데이터셋 | uspto-grants-1976_10 |
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| ORD ID | ord-02af007574754406b8dba1f3cb4ef1da |
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| 출처 메모 | uspto-grants-1976_10 |
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