Sodium Hydroxide → 2-(3-Bromo-5-chlorophenyl)acetic acid
反応式
C[O:2][C:3](=[O:17])[CH:4]([C:9]1[CH:14]=[C:13]([Cl:15])[CH:12]=[C:11]([Br:16])[CH:10]=1)C(OC)=O.[OH-].[Na+]>CO>[Br:16][C:11]1[CH:10]=[C:9]([CH2:4][C:3]([OH:17])=[O:2])[CH:14]=[C:13]([Cl:15])[CH:12]=1参加物
4
実験手順
2-(3-Bromo-5-chloro-phenyl)-malonic acid dimethyl ester (19 g, 59 mmol) in MeOH (500 mL) was treated with 1N aqueous NaOH (237 mL, 237 mmol) at 50° C. for 1.5 hours. The mixture was concentrated, and the residue was acidified and extracted twice with EtOAc. The combined organic layers were dried, filtered, and concentrated to give the title compound.
後処理
- concentrationThe mixture was concentrated
- extractionextracted twice with EtOAc
- customThe combined organic layers were dried
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-41b759f1484f40c1a41284429219fd41
- 出典データセット
- uspto-grants-2013_01
- 特許番号
- US08362044B2
反応ノート
読み込み中…