Hydrazine hydrate (1:1) → 3-Fluoro-4-phenylmethoxyaniline
反応式
O.NN.[CH2:4]([O:11][C:12]1[CH:17]=[CH:16][C:15]([N+:18]([O-])=O)=[CH:14][C:13]=1[F:21])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1>[Ni].CO>[CH2:4]([O:11][C:12]1[CH:17]=[CH:16][C:15]([NH2:18])=[CH:14][C:13]=1[F:21])[C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1参加物
5
実験手順
2.91 ml of hydrazine monohydrate and about 1 g of developed Raney nickel catalyst were added to a methanol (60 ml) solution of 4.94 g of 4-benzyloxy-3-fluoronitrobenzene, and the reaction liquid was stirred at room temperature for 2 hours. The catalyst was removed through filtration through Celite, and the solvent was evaporated away under reduced pressure to obtain the entitled compound as a yellow oily substance.
後処理
- customthe reaction liquid
- customThe catalyst was removed through filtration through Celite
- customthe solvent was evaporated away under reduced pressure
- customto obtain the entitled compound as a yellow oily substance
出典と根拠
- ORDレコード
- ord-8a7b2fe512ff448ba96e29c11a108f22
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07728025B2
反応ノート
読み込み中…