Benzenamine, 4-fluoro-N-hydroxy- → alpha-p-chlorophenyl-N-p-fluorophenylnitrone
反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][OH:9])=[CH:4][CH:3]=1.[Cl:10][C:11]1[CH:24]=[CH:23][C:14]([CH:15]=NC2C=CC=CC=2)=[CH:13][CH:12]=1>CCOCC>[Cl:10][C:11]1[CH:24]=[CH:23][C:14]([CH:15]=[N+:8]([C:5]2[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=2)[O-:9])=[CH:13][CH:12]=1参加物
4
実験手順
N-p-fluorophenylhydroxylamine (0.052 moles) was dissolved in ether (20 cc). This solution was treated with N-p-chlorobenzylideneaniline (0.05 moles) and dissolved in ether (50 cc). The product which separated was filtered and washed with ether to give α-p-chlorophenyl-N-p-fluorophenylnitrone.
後処理
- customThe product which separated
- filtrationwas filtered
- washwashed with ether
出典と根拠
- ORDレコード
- ord-bcccf3d29c8340c4877bfff89a06d8b8
- 出典データセット
- uspto-grants-1980_07
- 特許番号
- US04214003
反応ノート
読み込み中…