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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1018792생성일: 2026년 10월 26일

Isopropanol → 2-Amino-4-fluorophenol

https://huagongshe.com/reaction/1018792

반응식

참여 물질

역할이름HCID투입량
반응물IsopropanolHCID 3776—
반응물Propyl AcetateHCID 7997—
반응물4-Fluoro-2-nitrophenolHCID 136236—
반응물Potassium FormateHCID 2735122—
촉매PalladiumHCID 23938—
용매WaterHCID 962—
생성물2-Amino-4-fluorophenolHCID 273591791.2%

반응 단계

In a 500-ml flask, place 39.3 g (0.25 m) of 4-fluoro-2-nitrophenol (2a) and 120 ml of isopropyl alcohol and warm to 40° C. Add 1.5 g of 5% Pd/C wet with 1.5 ml of water and stir the mixture vigorously. Add a solution of 84.1 g (1.0 m) of potassium formate in 85 ml of water in drop wise over an hour keeping the temperature at 45°-53° C. Stir the mixture at 50° C. for 2.5 hrs. Add 150 ml of propyl acetate and 100 ml of water and stir for a few min. Filter off catalyst and wash with 100 ml of propyl acetate and 100 ml of water. Separate propyl acetate solution, and wash with 150 ml water and 150 ml of brine containing 1-2 g sodium hydrosulfite. Dry propyl acetate solution over magnesium sulfate and concentrate to approximately 75 ml. Add 300 ml of heptane slowly with gentle stirring. Concentrate under a reduced pressure till most of propyl acetate evaporated. Add 150 ml of heptane to resulting mush and cool in an ice bath for about an hour. Collect solid, wash with heptane, and dry in a vacuum oven to give 29.0 g (91%) of 2-amino-4-fluorophenol (3a; X=F) as gray solids.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06482985B1
출처 데이터셋uspto-grants-2002_11
ORD IDord-6b14a3d63e7046aaa4fa1c6fc2a3d9dd
출처 메모uspto-grants-2002_11