反応式
C(OC(C)(C)C)(=O)[NH:2][NH2:3].[CH3:10][C:11]1[O:15][C:14]([C:16](Cl)=[O:17])=[CH:13][CH:12]=1>C(Cl)Cl>[CH3:10][C:11]1[O:15][C:14]([C:16]([NH:2][NH2:3])=[O:17])=[CH:13][CH:12]=1参加物
4
実験手順
Tert-butyl carbazate (549 mg, 4.15 mmol) was added to a methylene chloride (10 mL) solution of commercially available 5-methylfuran-2-carbonyl chloride (500 mg, 3.46 mmol) under ice cooling, and the mixture was stirred at room temperature for 1 hour. The reaction solution was concentrated, and then, the residue was dissolved in methylene chloride (10 mL). To the solution, trifluoroacetic acid (2 mL) was added, and the mixture was stirred at room temperature for 1.5 hours. The reaction solution was concentrated to obtain 5-methylfuran-2-carbohydrazide.
後処理
- concentrationThe reaction solution was concentrated
- dissolutionthe residue was dissolved in methylene chloride (10 mL)
- additionTo the solution, trifluoroacetic acid (2 mL) was added
- stirringthe mixture was stirred at room temperature for 1.5 hours
- concentrationThe reaction solution was concentrated
出典と根拠
- ORDレコード
- ord-694b64273cac4806be76eab314deb09a
- 出典データセット
- uspto-grants-2013_06
- 特許番号
- US08466290B2
関連ノート
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