Sodium Hydroxide → 2-(4-Bromophenyl)-2-methylpropanoic acid
反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:15])([CH3:14])[C:9]([O:11]CC)=[O:10])=[CH:4][CH:3]=1.[OH-].[Na+]>O1CCCC1.CO>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([CH3:15])([CH3:14])[C:9]([OH:11])=[O:10])=[CH:6][CH:7]=1参加物
5
実験手順
To a solution of the product of Example 22A (3.7 g, 13.6 mmoles) in tetrahydrofuran (110.0 ml) and methanol (37.0 ml) was added 2 N sodium hydroxide (19.0 ml) and the solution was stirred at ambient temperature for about 16 hours. The reaction mixture was concentrated in vacuum down to the water layer, was cooled with an ice bath, and was acidified by addition of 2N hydrochloric acid. The precipitate was filtered off and was dried in vacuum to provide the title compound.
後処理
- concentrationThe reaction mixture was concentrated in vacuum down to the water layer
- temperaturewas cooled with an ice bath
- additionwas acidified by addition of 2N hydrochloric acid
- filtrationThe precipitate was filtered off
- customwas dried in vacuum
出典と根拠
- ORDレコード
- ord-e4fab534b8164ed0aefc0af450add9b5
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08198331B2
反応ノート
読み込み中…