反応式
[F:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.[NH2:11][C:12](=[N:18]O)[C:13]([O:15][CH2:16][CH3:17])=[O:14].C(N=C=NCCCN(C)C)C.C(OCC)C>CN(C)C1C=CN=CC=1.C(Cl)Cl>[NH2:18][C:12](=[N:11][O:7][C:6](=[O:8])[C:5]1[CH:9]=[CH:10][C:2]([F:1])=[CH:3][CH:4]=1)[C:13]([O:15][CH2:16][CH3:17])=[O:14]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
To a mixture of 4-fluorobenzoic acid (2.0 g), ethyl 2-amino-2-hydroxyiminoacetate (2.07 g) and 4-dimethylaminopyridine (0.52 g) in methylene chloride (30 ml) was added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (2.87 ml) at 0° C. under stirring. After stirring at ambient temperature for 1 hour, diethyl ether (10 ml) was added thereto and the resulting precipitate was filtered off, washed with diethyl ether, and dried in vacuo to give ethyl 2-amino-2-(4-fluorobenzoyloxyimino)acetate (3.2 g).
後処理
- stirringAfter stirring at ambient temperature for 1 hour
- filtrationthe resulting precipitate was filtered off
- washwashed with diethyl ether
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-2c9c36b844f840168efb45e7c85bf2f9
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05622976
関連ノート
読み込み中…