反応式
O1[C:5]2[CH:6]=[CH:7][C:8]([C:10]#[N:11])=[CH:9][C:4]=2[O:3][CH2:2]1.Cl.[NH2:13][OH:14].[OH-:15].[Na+]>CCO>[OH:14][NH:13][C:10]([C:8]1[CH:7]=[CH:6][C:5]2[O:15][CH2:2][O:3][C:4]=2[CH:9]=1)=[NH:11]参加物
5
実験手順
To a solution of Benzo[1,3]dioxole-5-carbonitrile (5.0 g, 33.9 mmol) in EtOH (100 mL) was added hydroxylamine hydrochloride (4.68 g, 67.90 mmol) and NaOH (2.71 g, 67.9 mmol). The resulting reaction mixture was refluxed for 12 h. After the completion of the reaction (TLC monitoring), the mixture was concentrated, added EtOH and filtered. The filtrate was evaporated under reduced pressure and used as such for the next step (crude yield 4.8 g, 78.68%).
後処理
- customThe resulting reaction mixture
- temperaturewas refluxed for 12 h
- customAfter the completion of the reaction (TLC monitoring)
- concentrationthe mixture was concentrated
- additionadded EtOH
- filtrationfiltered
- customThe filtrate was evaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-9b061b4b990849b49c3f77d2212db2d9
- 出典データセット
- uspto-grants-2012_01
- 特許番号
- US08088791B2
関連ノート
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