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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1018792Erstellt: 24. Oktober 2026

Isopropanol → 2-Amino-4-fluorophenol

https://huagongshe.com/de/reaction/1018792

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropanolHCID 3776—
EduktPropyl AcetateHCID 7997—
Edukt4-Fluoro-2-nitrophenolHCID 136236—
EduktPotassium FormateHCID 2735122—
KatalysatorPalladiumHCID 23938—
LösungsmittelWaterHCID 962—
Produkt2-Amino-4-fluorophenolHCID 273591791,2%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06482985B1
Quelldatensatzuspto-grants-2002_11
ORD IDord-6b14a3d63e7046aaa4fa1c6fc2a3d9dd
Quellennotizuspto-grants-2002_11