反応式
Cl.[NH2:2][C:3]1[C:8]([OH:9])=[CH:7][CH:6]=[CH:5][C:4]=1[OH:10].[C:11](OC)(OC)(OC)C>S(=O)(=O)(O)O>[O:9]1[C:8]2=[CH:7][CH:6]=[CH:5][C:4]([OH:10])=[C:3]2[N:2]=[CH:11]1参加物
4
実験手順
A mixture of 2-amino-benzene-1,3-diol hydrochloride (2.00 g, 12.4 mmol) and trimethyl orthoacetate (15 mL) was treated with concentrated sulfuric acid (5 drops) and the resulting mixture heated at reflux for 3 h, cooled and allowed to stand at room temperature overnight. The resulting mixture was concentrated in vacuo and the residue treated with ethyl acetate (200 mL), washed with water (200 mL) and brine (100 mL). The combined aqueous phases were extracted with ethyl acetate (200 mL) and the combined organic phases washed with brine and dried over sodium sulfate. The mixture was filtered and concentrated in vacuo which afforded benzooxazol-4-ol (0.94 g, 51%) as a yellow solid.
後処理
- temperaturethe resulting mixture heated
- temperatureat reflux for 3 h
- temperaturecooled
- concentrationThe resulting mixture was concentrated in vacuo
- additionthe residue treated with ethyl acetate (200 mL)
- washwashed with water (200 mL) and brine (100 mL)
- extractionThe combined aqueous phases were extracted with ethyl acetate (200 mL)
- washthe combined organic phases washed with brine
- dry with materialdried over sodium sulfate
- filtrationThe mixture was filtered
- concentrationconcentrated in vacuo which
出典と根拠
- ORDレコード
- ord-e80020f93f3445a18bd2b839f88c261b
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07741327B2
関連ノート
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