Hydrochloric Acid → 4-Chloro-2-[2-(dimethylamino)-2-oxoethoxy]benzoic acid
反応式
[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([C:6]([O:8]CC(N(C)C)=O)=[O:7])=[C:4]([O:17][CH2:18][C:19]([N:21]([CH3:23])[CH3:22])=[O:20])[CH:3]=1.CO.O[Li].O.Cl>O.C(OCC)(=O)C>[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([C:6]([OH:8])=[O:7])=[C:4]([O:17][CH2:18][C:19]([N:21]([CH3:23])[CH3:22])=[O:20])[CH:3]=1参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
The product from step (v) (1.0 g) was dissolved in a 2:1 water: methanol mixture (15 ml) and LiOH.H2O added. After 2 hours 2M aqueous HCl solution and ethyl acetate were added, the organic phase separated, dried and concentrated to give the sub-titled product as a solid (1.2 g).
後処理
- customthe organic phase separated
- customdried
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-f1e2653055c140a89037e3d16d2d3cd0
- 出典データセット
- uspto-grants-2003_02
- 特許番号
- US06518286B1
反応ノート
読み込み中…