反応式
Cl.[NH2:2][C:3]1[C:9]([OH:10])=[CH:8][CH:7]=[CH:6][C:4]=1[OH:5].O.[CH2:12](O)C>>[OH:10][C:9]1[C:3]2[N:2]=[CH:12][O:5][C:4]=2[CH:6]=[CH:7][CH:8]=1参加物
4
実験手順
2-Aminoresorcinol hydrochloride (2 g) and triethylchloroformate (4.5 ml) were heated to reflux under nitrogen for 3 h. After cooling to room temperature, the reaction mixture was poured into a mixture of water (70 ml) and ethanol (20 ml). The mixture was stirred vigorously for 30 minutes, then left to stand at room temperature overnight. The beige precipitate which formed was collected by filtration, and dried by azeotroping with toluene to give the title compound as a beige solid (1.2 g).
後処理
- temperatureto reflux under nitrogen for 3 h
- waitleft
- waitto stand at room temperature overnight
- customThe beige precipitate which formed
- filtrationwas collected by filtration
- customdried
- customby azeotroping with toluene
出典と根拠
- ORDレコード
- ord-88646d822d164a579bb5c38570591b6e
- 出典データセット
- uspto-grants-2002_03
- 特許番号
- US06353010B1
関連ノート
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