戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1687824作成日:2026年10月26日

Methanol → 2-(3-Methoxyphenyl)-2-methylpropanoic acid

https://huagongshe.com/reaction/1687824

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Potassium HydroxideHCID 14797—
反応物2-(3-Methoxyphenyl)-2-methylpropanenitrileHCID 10130193—
溶媒WaterHCID 962—
生成物2-(3-Methoxyphenyl)-2-methylpropanoic acidHCID 10821634—

反応条件

温度130 °C

反応手順

Into a round bottom flask, potassium hydroxide (35.4 g, 631 mmol) and water (225 mL, 12500 mmol) was added at 100° C. 2-(3-methoxy-phenyl)-2-methyl-propionitrile (44.20 g, 252.2 mmol) in Methanol (25.0 mL, 617 mmol) was added to the reaction mixture. The reaction was then heated to reflux at 130° C. over night. TLC suggested starting material. Potassium hydroxide (35.4 g, 631 mmoles) in water (50 mL) was added. The reaction was heated for 5 days. The reaction was partitioned with water (700 mL). The aqueous was acidified with concentrated HCl to pH 1. The solid was filtered and washed with water and EtOAc. The organic layer was separated. The aqueous was extracted with EtOAc (3×400 mL). The combined organic was washed with brine, and dried over MgSO4. The solid was then filtered and washed with EtOAc. The solvent was removed under vacuum to afford a brown oil. The oil was triturated with hexane to afford 2-(3-methoxy-phenyl)-2-methyl-propionic acid as a light yellow solid (36.2 g. 74%). H-NMR (DMSO-D6, 400 MHz): δ 12.30 (s, 1H), 7.24 (t, 1H), 6.90 (d, 1H), 6.75-6.88 (m, 2H), 3.74 (s, 3H), 1.45 (s, 6H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08148391B2
出典データセットuspto-grants-2012_04
ORD IDord-044104c248124cfb86e3eafcf377d2ee
出典メモuspto-grants-2012_04