참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Pentanenitrile, 4,4-dimethyl-3-oxo- | HCID 108871 | — |
| 반응물 | Hydroxylamine, sulfate (1:1) | HCID 159255 | — |
| 촉매 | Sulfuric Acid | HCID 1118 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 3-Isoxazolamine, 5-(1,1-dimethylethyl)- | HCID 171473 | 125.1% |
반응 단계
To a suspension of pivaloylacetonitrile (25.03 g) in water (400 ml) is added 96% sodium hydroxide (9.17 g). Hydroxylamine sulfate (18.06 g) is added to the resulting solution at 27° C. The mixture is stirred at room temperature for 30 minutes, adjusted to pH 8 with 10% sulfuric acid (0.97 g), stirred at 60° C. for 22 hours, cooled at 20° C., mixed with conc. hydrochloric acid (7.90 g), and heated at 50° C. for 2 hours. Conc. hydrochloric acid (14.18 g) is added to the mixture, which is heated at 100° C. for 1 hour. After cooling, the reaction mixture is adjusted to pH 11 with 30% sodium hydroxide (49.8 g) and shaken with chloroform. The organic layer is washed with water, dried over anhydrous sodium sulfate and concentrated to remove chloroform, whereby 3-amino-5-t-butylisoxazole (24.16 g) is obtained. Yield, 86.2%. Purity, 95.4%. m.p. 103.5-109° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04256899 |
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| 출처 데이터셋 | uspto-grants-1981_03 |
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| ORD ID | ord-b4908edb535c4a73bfe5fb627436f4d4 |
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| 출처 메모 | uspto-grants-1981_03 |
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