돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32868생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/32868

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Acetamidomalonic acid diethyl esterHCID 14041—
반응물Sodium hydrideHCID 24758—
반응물Bis(4-fluorophenyl)methylene chlorideHCID 12714043—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물2-Acetylamino-3,3-bis(4-fluorophenyl)propanoic acidHCID 11977829104.4%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427688B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-6327e9d4ebee4f9e8e5a095143209a8b
출처 메모uspto-grants-2008_09