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HRID 605136作成日:2026年10月25日

Trifluoroacetic acid → 4-(4-Amino-phenoxy)-N-(4-bromo-phenyl)-3-nitro-benzamide

https://huagongshe.com/reaction/605136

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物{4-[4-(4-Bromo-phenylcarbamoyl)-2-nitro-phenoxy]phenyl}-carbamic acid tert-butyl esterHCID 67040702—
溶媒DichloromethaneHCID 6344—
生成物4-(4-Amino-phenoxy)-N-(4-bromo-phenyl)-3-nitro-benzamideHCID 6704050697.2%

反応手順

A solution of the product of Example 10B (250 mg, 0.4732 mmol) in methylene chloride (5 mL) was treated with trifluoroacetic acid (5 mL) at room temperature for 30 minutes. The solvents were removed by rotary evaporation under vacuum, and the residue taken up in ethyl acetate (100 mL) and washed with saturated aqueous sodium hydrogen carbonate (2×50 mL), water (50 mL), and brine (50 mL). The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum to provide the title compound as a light orange solid (197 mg, 97%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07910595B2
出典データセットuspto-grants-2011_03
ORD IDord-ab2b9c3289ac4e2fa2c278a73a4f920c
出典メモuspto-grants-2011_03