Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Isopropanol | HCID 3776 | — |
| Edukt | Propyl Acetate | HCID 7997 | — |
| Edukt | 4-Fluoro-2-nitrophenol | HCID 136236 | — |
| Edukt | Potassium Formate | HCID 2735122 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-Amino-4-fluorophenol | HCID 2735917 | 91,2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06482985B1 |
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| Quelldatensatz | uspto-grants-2002_11 |
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| ORD ID | ord-6b14a3d63e7046aaa4fa1c6fc2a3d9dd |
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| Quellennotiz | uspto-grants-2002_11 |
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