Sodium Hydroxide → 5-Benzofuranacetic acid
反応式
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][C:11]([O:13]C)=[O:12])=[CH:9][C:4]=2[CH:3]=[CH:2]1.[OH-].[Na+]>CO>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][C:11]([OH:13])=[O:12])=[CH:9][C:4]=2[CH:3]=[CH:2]1参加物
4
実験手順
Methyl benzofuran-5-ylacetate (1.2 gm, 6.3 mmol) was dissolved in methanol (10 mL) and 2N sodium hydroxide (6.5 mL) was added under nitrogen and the mixture was stirred at rt for 3 hr. It was then diluted-with water and extracted with ether. The aqueous layer was acidified with 2N hydrochloric acid and again extracted twice with ethyl acetate. The organic layers were washed with brine, combined, dried over sodium sulfate and evaporated to give 1.1 gm of title compound suitable for the next step.
後処理
- extractiondiluted-with water and extracted with ether
- extractionagain extracted twice with ethyl acetate
- washThe organic layers were washed with brine
- dry with materialdried over sodium sulfate
- customevaporated
出典と根拠
- ORDレコード
- ord-e1f85173cb4b40e7912ff01baf9a6454
- 出典データセット
- uspto-grants-1995_05
- 特許番号
- US05420010
反応ノート
読み込み中…