4-(4-Chloro-2-fluoro-phenoxy)-3-fluoro-benzonitrile → 4-(4-Chloro-2-fluoro-phenoxy)-3-fluoro-benzylamine
반응식
[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:14]=[CH:13][C:10]([C:11]#[N:12])=[CH:9][C:8]=2[F:15])=[C:4]([F:18])[CH:3]=1>N.[Ni]>[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:14]=[CH:13][C:10]([CH2:11][NH2:12])=[CH:9][C:8]=2[F:15])=[C:4]([F:18])[CH:3]=1참가 물질
4
실험 절차
1.0 g (3.76 mmol) of 4-(4-chloro-2-fluoro-phenoxy)-3-fluoro-benzonitrile were hydrogenated in 30 mL methanolic ammonia solution with the addition of Raney nickel at 50° C. under a hydrogen pressure of 50 psi. Then the catalyst was filtered off and the filtrate was evaporated to dryness. The crude product thus obtained was reacted further without any further purification.
후처리
- filtrationThen the catalyst was filtered off
- customthe filtrate was evaporated to dryness
출처 및 근거
- ORD 기록
- ord-e937f86b4fdf4fd49a4a5821587aecaa
- 출처 데이터셋
- uspto-grants-2014_12
- 특허 번호
- US08916589B2
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