Sodium Hydroxide → 7-Chloro-1-benzothiophene-2-carboxylic acid
反応式
[Cl:1][C:2]1[C:7]2[S:8][C:9]([C:11]([O:13]C)=[O:12])=[CH:10][C:6]=2[CH:5]=[CH:4][CH:3]=1.[OH-].[Na+]>C(O)C>[Cl:1][C:2]1[C:7]2[S:8][C:9]([C:11]([OH:13])=[O:12])=[CH:10][C:6]=2[CH:5]=[CH:4][CH:3]=1参加物
4
実験手順
Methyl 7-chlorobenzo[b]thiophene-2-carboxylate (3 g, 13 mmol) was dissolved is ethanol (15 mL) and treated 5 N sodium hydroxide (5 mL). The reaction was heated at reflux overnight. The volatiles were removed in vacuo and the aqueous residue was acidified to pH 2 using 5 N HCl. The resulting white solid was filtered off, washed well with water and dried in a vacuum oven at 60° C. Yield=2.6 g. MS (M−H)− 210.
後処理
- temperatureThe reaction was heated
- temperatureat reflux overnight
- customThe volatiles were removed in vacuo
- filtrationThe resulting white solid was filtered off
- washwashed well with water
- customdried in a vacuum oven at 60° C
出典と根拠
- ORDレコード
- ord-fea189dc2932427e8c75b27d77b41223
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07786132B2
反応ノート
読み込み中…