反応式
S([O-])([O-])(=O)=O.[Na+].[Na+].[OH2:8].Cl[C:10](Cl)(Cl)[CH:11]=[O:12].[NH2:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][CH2:23][N:24]2[CH2:28][CH2:27][O:26][C:25]2=[O:29])=[CH:18][CH:17]=1.Cl.[NH2:31]O>O.Cl>[OH:8][N:31]=[CH:10][C:11]([NH:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][CH2:23][N:24]2[CH2:28][CH2:27][O:26][C:25]2=[O:29])=[CH:18][CH:17]=1)=[O:12]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
Sodium sulphate (78.3 g) is added to a solution of trichloroacetaldehyde hydrate (32.5 mmoles) in water (100 ml). To the resulting suspension there are added a solution of 3-[2-(4-amino-phenyl)ethyl]oxazolidin-2-one in water (20 ml) and concentrated HCl solution (2.83 ml). A solution of hydroxylamine hydrochloride (95 mmoles) in water (50 ml) is then added. The reaction mixture is heated at reflux for two hours. The mixture is then cooled to ambient temperature. The solid formed is then filtered off, washed with water and dried in vacuo in the presence of P2O5 and at 40° C. overnight to yield the title product, which is used directly in the next Step.
後処理
- temperatureThe reaction mixture is heated
- temperatureat reflux for two hours
- customThe solid formed
- filtrationis then filtered off
- washwashed with water
- dry with materialdried in vacuo in the presence of P2O5 and at 40° C. overnight
出典と根拠
- ORDレコード
- ord-64e59fa5f1e24f38bf1b501021197d01
- 出典データセット
- uspto-grants-2014_02
- 特許番号
- US08653073B2
関連ノート
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