戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 219774作成日:2026年10月26日

Sodium Hydroxide → 3-Methyl-4-[2-(trifluoromethyl)phenyl]benzoic acid

https://huagongshe.com/reaction/219774

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Methyl 2-methyl-2'-(trifluoromethyl)biphenyl-4-carboxylateHCID 59606539—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物3-Methyl-4-[2-(trifluoromethyl)phenyl]benzoic acidHCID 2194781284%

反応条件

温度60 °C

反応手順

To a solution of methyl 2-methyl-2′-(trifluoromethyl)biphenyl-4-carboxylate, prepared in step 1 (3 g; 10.19 mmol; 1 eq.) in EtOH (90 mL), was added at RT an aqueous solution of sodium hydroxide (6.12 mL; 5 M; 30.58 mmol; 3 eq.). The reaction mixture was stirred at 60° C. for one hour. The reaction mixture was concentrated under vacuum to give a brown solid. It was taken up in water (400 mL) and the aqueous phase was washed twice with EtOAc (200 mL). Aqueous phase was acidified with concentrated HCl (2 mL) to pH 2. Then it was concentrated under vacuum until a precipitate was formed (⅓ of volume). The suspension was filtered off and dried under vacuum, affording the title compound as a beige solid (2.41 g, 84%). 1H NMR: (DMSO-d6, 300 MHz) δ 13.03 (s, 1H), 7.91-7.68 (m, 5H), 7.38-7.36 (d, J=8.27 Hz, 1H), 7.27-7.25 (d, J=8.24 Hz, 1H), 2.05 (s, 3H). LC/MS (Method A): 279.0 (M−H)−. HPLC (Method A) Rt 4.49 min (Purity: 95.7%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202865B2
出典データセットuspto-grants-2012_06
ORD IDord-50b1b3cf03a945c0a25f99461b0a7743
出典メモuspto-grants-2012_06