Ammonium Hydroxide → 2-Amino-3,6-difluorobenzonitrile
反応式
F[C:2]1[C:9]([F:10])=[CH:8][CH:7]=[C:6]([F:11])[C:3]=1[C:4]#[N:5].[OH-].[NH4+:13]>C(#N)C>[NH2:13][C:2]1[C:9]([F:10])=[CH:8][CH:7]=[C:6]([F:11])[C:3]=1[C:4]#[N:5]参加物
4
実験手順
2,3,6-Trifluorobenzonitrile (15 g) in ammonium hydroxide solution (28% in water; 80 mL) and acetonitrile (40 mL) was stirred at 70° C. in a pressure vessel for 16 h and the reaction was complete based on GC-MS. Acetonitrile was removed under reduced pressure, and water was added. The white solid precipitate was suction filtered, washed with water and dried under house vacuum over a weekend at room temperature to give 13.7 g (93%) of the crude product; M.P. 90-92° C. GC/MS: m/z 154. 1H NMR (CDCl3): δ 7.07-7.16 (m, 1H), 6.36-6.43 (m, 1H), 4.65 (br s, 2H).
後処理
- customAcetonitrile was removed under reduced pressure, and water
- additionwas added
- filtrationfiltered
- washwashed with water
- customdried under house vacuum over a weekend at room temperature
出典と根拠
- ORDレコード
- ord-02f7ad8131d74654b2ef8df1b585631f
- 出典データセット
- uspto-grants-2012_09
- 特許番号
- US08268843B2
反応ノート
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