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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59636Generated: October 24, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminophenolHCID 5801—
Reactant2-MethyltetrahydrofuranHCID 7301—
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantDiosgeninHCID 99474—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
Product4-Fluoro-N-(2-hydroxyphenyl)benzamideHCID 579383—

Reaction Conditions

Temperature60 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440935B2
Source datasetuspto-grants-2016_09
ORD IDord-184b04ec7f5642aabf0759c1f6f1a299
Source noteuspto-grants-2016_09