Formaldehyde → 3-(3-Bromo-4-chlorophenyl)thiazolidin-4-one
反応式
[C:1]([OH:5])(=O)[CH2:2][SH:3].[CH2:6]=O.[Br:8][C:9]1[CH:10]=[C:11]([CH:13]=[CH:14][C:15]=1[Cl:16])[NH2:12]>C1(C)C=CC=CC=1>[Br:8][C:9]1[CH:10]=[C:11]([N:12]2[C:1](=[O:5])[CH2:2][S:3][CH2:6]2)[CH:13]=[CH:14][C:15]=1[Cl:16]参加物
5
実験手順
Thioglycolic acid (8.65 g) and 37% aqueous formaldehyde (4.6 ml) was added to a stirred solution of 3-bromo-4-chloroaniline (9.73 g) in toluene (50 ml). The mixture was heated to reflux and the water collected in a Dean and Stark apparatus. After 3 hours the mixture was cooled, diluted with toluene then washed with aqueous sodium hydroxide and water. The organic layer was dried (MgSO4) and concentrated to give the subtitle compound as a solid.
後処理
- temperatureThe mixture was heated
- temperatureto reflux
- customthe water collected in a Dean and Stark apparatus
- temperatureAfter 3 hours the mixture was cooled
- additiondiluted with toluene
- washthen washed with aqueous sodium hydroxide and water
- dry with materialThe organic layer was dried (MgSO4)
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-55f5dd449ef5494aac677a1f07786f7f
- 出典データセット
- uspto-grants-2000_02
- 特許番号
- US06022976
反応ノート
読み込み中…