2,4,6-Trimethoxybenzonitrile → N-HYDROXY-2,4,6-TRIMETHOXY-BENZAMIDINE
反応式
Cl.[NH2:2][OH:3].CC[O-].[Na+].[Na].[CH3:9][O:10][C:11]1[CH:18]=[C:17]([O:19][CH3:20])[CH:16]=[C:15]([O:21][CH3:22])[C:12]=1[C:13]#[N:14]>C(O)C>[CH3:22][O:21][C:15]1[CH:16]=[C:17]([O:19][CH3:20])[CH:18]=[C:11]([O:10][CH3:9])[C:12]=1[C:13](=[N:2][OH:3])[NH2:14]参加物
6
実験手順
To a suspension of 13.8 g of hydroxylamine hydrochloride in 100 ml of ethanol is added, at a temperature in the region of 15° C., a solution of NaOC2H5 prepared by dissolving 4.3 g of sodium in 100 ml of ethanol. 12 g of 2,4,6-trimethoxybenzonitrile are introduced into the medium, followed by heating at reflux for 41 h before evaporating to dryness. The crystals are washed with water and with dichloromethane.
後処理
- additionis added, at a temperature in the region of 15° C.
- temperatureby heating
- temperatureat reflux for 41 h
- custombefore evaporating to dryness
- washThe crystals are washed with water and with dichloromethane
出典と根拠
- ORDレコード
- ord-6d38f2833779447cbd4d3dbb4de43b23
- 出典データセット
- uspto-grants-1996_07
- 特許番号
- US05534530
反応ノート
読み込み中…