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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 59636Erstellt: 23. Oktober 2026

2-Aminophenol → 4-Fluoro-N-(2-hydroxyphenyl)benzamide

https://huagongshe.com/de/reaction/59636

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminophenolHCID 5801—
Edukt2-MethyltetrahydrofuranHCID 7301—
Edukt4-Fluorobenzoyl chlorideHCID 67879—
EduktDiosgeninHCID 99474—
EduktSodium BicarbonateHCID 516892—
LösungsmittelWaterHCID 962—
Produkt4-Fluoro-N-(2-hydroxyphenyl)benzamideHCID 579383—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a 500 ml 4 necked round bottom flask equipped with a thermometer, a mechanic stirrer, a drop funnel, a nitrogen in-let, was added sodium bicarbonate (29.6 g, 0.354 mol, 1.1 eq), 2-aminophenol (34.88 g, 0.32 mol, 1 eq) and 2-Methyl THF (250 ml). The temperature of the mixture was controlled under 20° C. by ice-bath. Under vigorously stirring, 4-fluorobenzoyl chloride (50.72 g, 0.32 mol, 1 eq) was added drop wise within 10 min. Then the reaction was allowed to be stirred for another 1.5 hrs. When HPLC data showed that less than 0.3% of 2-aminophenol remained, 100 ml of water and 50 ml of 2-methyl tetrahydrofuran was added to quench the reaction and then the mixture was heated to 60° C. with stirring. The mixture was partitioned into two phases and the organic phase was washed with 100 ml of 1N H2SO4 and subsequently with 100 ml of water. Then the solvent was evaporated to almost dryness with stirring.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440935B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-184b04ec7f5642aabf0759c1f6f1a299
Quellennotizuspto-grants-2016_09