(2-Amino-4-chlorophenyl)methanol → 2-Amino-4-chlorobenzaldehyde
反応式
[NH2:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH2:9][OH:10]>C(Cl)(Cl)Cl.[O-2].[O-2].[Mn+4]>[NH2:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH:9]=[O:10]参加物
4
実験手順
(2-amino-4-chlorophenyl)methanol (10.08 g, 64.0 mmol) was suspended in chloroform (250 mL) and treated with manganese dioxide (15.87 g, 183 mmol). The mixture was stirred vigorously and heated at reflux. The oxidation was followed by TLC and found to be complete after 1 hour. The suspension was filtered through a pad of CELITE™ and evaporated to dryness under reduced pressure. Further drying under high vacuum gave a dark red solid which was used in the next step without further purification.
後処理
- temperatureheated
- temperatureat reflux
- filtrationThe suspension was filtered through a pad of CELITE™
- customevaporated to dryness under reduced pressure
- customFurther drying under high vacuum
- customgave a dark red solid which
- customwas used in the next step without further purification
出典と根拠
- ORDレコード
- ord-2cf16fb38d554c9fa404efcf50bdba68
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09174992B2
反応ノート
読み込み中…