Hydrochloric Acid → 5-(Trifluoromethyl)isoxazol-3-ylamine
反応式
[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]=1参加物
4
実験手順
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.
後処理
- customThe product was then purified by column chromatography on silica gel
- distillationfurther distilled under reduced pressure
出典と根拠
- ORDレコード
- ord-b16fdf4684a24f6ca2d8325886bfd4fa
- 出典データセット
- uspto-grants-1989_01
- 特許番号
- US04797492
反応ノート
読み込み中…