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HRID 1018792作成日:2026年10月26日

Isopropanol → 2-Amino-4-fluorophenol

https://huagongshe.com/reaction/1018792

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物Propyl AcetateHCID 7997—
反応物4-Fluoro-2-nitrophenolHCID 136236—
反応物Potassium FormateHCID 2735122—
触媒PalladiumHCID 23938—
溶媒WaterHCID 962—
生成物2-Amino-4-fluorophenolHCID 273591791.2%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06482985B1
出典データセットuspto-grants-2002_11
ORD IDord-6b14a3d63e7046aaa4fa1c6fc2a3d9dd
出典メモuspto-grants-2002_11