Hydrochloric Acid → 5-(Trifluoromethyl)isoxazol-3-ylamine
반응식
[F:1][C:2]([F:13])([F:12])[C:3]1[O:7][N:6]=[C:5]([NH:8]C(=O)C)[CH:4]=1.Cl>C(O)CO>[F:1][C:2]([F:13])([F:12])[C:3]1[O:7][N:6]=[C:5]([NH2:8])[CH:4]=1참가 물질
4
실험 절차
The reaction was carried out according to the same procedure as described in Example 50 except that 5-trifluoromethyl-3-acetylaminoisoxazole (2.21 g, 11.4 mmole), 36% hydrochloric acid (2.89 g, 28.5 mmole) and ehtylene glycol (11.4 ml) were used. The product was then purified by column chromatography on silica gel and further distilled under reduced pressure to give the title compound. Yield: 1.22 g (70.4%), b.p. 84°-85° C./13.0 mmHg.
후처리
- customThe product was then purified by column chromatography on silica gel
- distillationfurther distilled under reduced pressure
출처 및 근거
- ORD 기록
- ord-b16fdf4684a24f6ca2d8325886bfd4fa
- 출처 데이터셋
- uspto-grants-1989_01
- 특허 번호
- US04797492
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