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HRID 393328作成日:2026年10月25日

Acetic Acid → 2-amino-5-(trifluoromethoxy)benzoic Acid

https://huagongshe.com/reaction/393328

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Hydrogen PeroxideHCID 784—
反応物Potassium HydroxideHCID 14797—
反応物5-(trifluoromethoxy)-2,3-dihydro-1H-indole-2,3-dioneHCID 2732752—
溶媒WaterHCID 962—
生成物2-amino-5-(trifluoromethoxy)benzoic AcidHCID 1108534987%

反応条件

温度0 °C

反応手順

5-(Trifluoromethoxy)isatin (15.0 g, 65 mmol) and potassium hydroxide pellets (4 g) were mixed in water (35 mL) and cooled to 0° C. With vigorous stirring, a solution of 30% aqueous hydrogen peroxide (11.7 g), potassium hydroxide pellets (5.8 g), and water (80 mL) was added drop-wise keeping the temperature below 10° C. After stirring 1 hour at 0 C, glacial acetic acid (22 mL) was added drop-wise, causing foaming and formation of a precipitate. The contents were stirred overnight and filtered to afford the 2-amino-5-trifluoromethoxybenzoic acid as an amber solid (12.5 g, 87%). A small amount was recrystallized from ethyl acetate-hexanes to afford amber needles for an analytical sample and the remaining compound was used without further purification: mp 142.5-144.2° C. 1H NMR (CDCl3, 300 MHz) 7.98 (s, 1H), 7.18 (d, 1H, J=8.0 Hz), 6.62 (d, 1H, J=8.0 Hz), 6.40 (brs, 2H). Anal. Calc'd for C8H6NO3F3: C, 43.45; H, 2.73; N, 6.33. Found: C, 43.40; H, 2.65; N, 6.35.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06806288B1
出典データセットuspto-grants-2004_10
ORD IDord-ac6960d965da462a9997d1fee0423cfd
出典メモuspto-grants-2004_10