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HRID 32868作成日:2026年10月26日

Potassium Iodide → 2-Acetylamino-3,3-bis(4-fluorophenyl)propanoic acid

https://huagongshe.com/reaction/32868

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Acetamidomalonic acid diethyl esterHCID 14041—
反応物Sodium hydrideHCID 24758—
反応物Bis(4-fluorophenyl)methylene chlorideHCID 12714043—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物2-Acetylamino-3,3-bis(4-fluorophenyl)propanoic acidHCID 11977829104.4%

反応手順

To a solution of diethyl acetamidomalonate (22.79 g, 105.4 mmol) in N-methyl-2-pyrrolidone (84 mL) was added 55% sodium hydride (4.58 g, 105.2 mmol), and the mixture was stirred at room temperature for 1 hr. Bis(4-fluorophenyl)methylene chloride (16.5 mL, 84.7 mmol) and potassium iodide (13.95 g, 84.0 mmol) were added, and the mixture was stirred at 50° C. for 5 hrs. After completion of the reaction, toluene (200 mL) and water (100 mL) were added to the reaction mixture, and the mixture was partitioned. The obtained organic layer was washed twice with water (100 mL) and concentrated. Ethanol (108 mL) and 2M aqueous sodium hydroxide solution (127 mL) were added to the concentrated solution, and the mixture was stirred at 90° C. for 2.5 hrs. The reaction mixture was allowed to cool to 25° C., toluene (200 mL) and water (50 mL) were added, and the mixture was partitioned. The aqueous layer was concentrated to a half volume, and isopropyl acetate (60 mL) and water (130 mL) were added. The mixture was adjusted to pH 1.1 with concentrated hydrochloric acid and partitioned. The organic layer was washed with water (200 mL), concentrated and dried under vacuum to give the title compound (28.24 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07427688B2
出典データセットuspto-grants-2008_09
ORD IDord-6327e9d4ebee4f9e8e5a095143209a8b
出典メモuspto-grants-2008_09