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HRID 1725218作成日:2026年10月27日

Acetic Acid → N-{[4-(Trifluoromethoxy)phenyl]methyl}acetamide

https://huagongshe.com/reaction/1725218

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物DiisopropylethylamineHCID 81531—
反応物4-(Trifluoromethoxy)benzylamineHCID 571846—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物N-{[4-(Trifluoromethoxy)phenyl]methyl}acetamideHCID 4454270792%

反応手順

To a solution of 4-(trifluoromethoxy)benzylamine (3.46 g, 57.6 mmol) in DMF (75 mL) and acetic acid (10.0 g, 52.3 mmol) at −10° C. were added O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (20.2 g, 62.8 mmol) and N,N-diisopropylethylamine (20.0 mL, 115 mmol) and the reaction mixture was stirred at room temperature overnight. Ethyl acetate (200 mL) was added and the organic phase was washed with water (100 mL), 0.25 M NaOH (100 mL), saturated aqueous NaHCO3 (100 mL), water (100 mL), 0.5 M HCl (100 mL), and water (100 mL), dried over MgSO4, and concentrated in vacuo to afford 11.2 g (92%) of a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07488844B2
出典データセットuspto-grants-2009_02
ORD IDord-99f12c5549444f3faedccd5ccca03911
出典メモuspto-grants-2009_02