反応式
[Cl:1][C:2]1[NH:3][N:4]=[C:5]2[C:10]=1[CH:9]=[CH:8][CH:7]=[CH:6]2.[CH2:11]=[O:12]>O>[Cl:1][C:2]1[N:3]([CH2:11][OH:12])[N:4]=[C:5]2[C:10]=1[CH:9]=[CH:8][CH:7]=[CH:6]2参加物
4
実験手順
In a 250 mL round bottom flask, 3-chloro-2H-indazole (1.95 g, 10 mmol), 30% HCHO (2 mL, 20 mmol) were mixed in water (10 mL). The reaction mixture was refluxed for 2 hours. After cooling down to room temperature, the solid was filtered, washed with water, and dried under vacuum to provide (3-chloro-2H-indazol-2-yl)methanol (1.82 g, 99% yield).
後処理
- temperatureThe reaction mixture was refluxed for 2 hours
- filtrationthe solid was filtered
- washwashed with water
- customdried under vacuum
出典と根拠
- ORDレコード
- ord-df448b7d99c644bc9ce7349e01de42a3
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09315521B2
関連ノート
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