戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 517533作成日:2026年10月26日

4-(Trifluoromethoxy)benzonitrile → 4-(Trifluoromethoxy)benzamidoxime

https://huagongshe.com/reaction/517533

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Trifluoromethoxy)benzonitrileHCID 67621—
反応物Hydroxyamine hydrochlorideHCID 443297—
溶媒EthanolHCID 702—
生成物4-(Trifluoromethoxy)benzamidoximeHCID 273330985.7%

反応手順

To a solution of 4-(trifluoromethoxy)benzonitrile (2.0 g, 10.6 mmol) in EtOH (20 mL), TEA (53 g, 53.0 mmol) and NH2OH.HCl (3.6 g, 26.5 mmol) were added in sequence. The mixture was refluxed for 4 h, cooled to RT, and concentrated under reduced pressure. The residue was diluted with H2O (20 mL), and extracted with EtOAc (20 mL×3). The combined organic layers were washed with H2O (1×10 mL) and brine (1×10 mL), dried over Na2SO4, filtered and concentrated to afford the crude N-hydroxy-4-(trifluoromethoxy)benzimidamide (2.0 g, 85%), which was directly used for next reaction without further purification. MS (ES+) C8H7F3N2O2 requires: 220, found: 221 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115120B2
出典データセットuspto-grants-2015_08
ORD IDord-1757aedbb7e148678fc16b7dedc8448d
出典メモuspto-grants-2015_08