Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 372499Erstellt: 25. Oktober 2026

Hydrochloric Acid → 2',4-Dihydroxy-3,5-dimethylbenzanilide

https://huagongshe.com/reaction/372499

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktAspirinHCID 2244—
EduktN,N'-DicyclohexylureaHCID 4277—
EduktDicyclohexylcarbodiimideHCID 10868—
EduktSodium HydroxideHCID 14798—
Edukt4-Amino-2,6-dimethylphenolHCID 82668—
LösungsmittelEthylene GlycolHCID 174—
LösungsmittelAcetoneHCID 180—
Produkt2',4-Dihydroxy-3,5-dimethylbenzanilideHCID 20327558—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Acetylsalicylic acid (50 mg.) and 4-amino-2,6-dimethylphenol (38 mg.) were dissolved in ethylene glycol (5 ml.) to which under cooling at 0° C. was added dicyclohexyl carbodiimide (65 mg.). After reaction for several hours the formed dicyclohexylurea was filtered off and the filtrate evaporated to dryness to give a powder which was dissolved in acetone (2 ml.); after adding 2 N sodium hydroxide (4 ml.), the solution was allowed to stand for several hours at room temperature. The addition of 2 N hydrochloric acid (20 ml.) gave a precipitate which was collected by filtration, washed with water and dried at 50° C. under reduced pressure to give solid 2',4-dihydroxy-3,5-dimethylbenzanilide as a powder which was then purified by column chromatography using Sephadex LH-20 resin and elution with methanol. The eluate was evaporated to dryness to give a solid which was recrystallized from aqueous acetone to give white crystals (57.8 mg.) of 2',4-dihydroxy-3,5-dimethylbenzanilide. Yield: 80.9%. Melting point: 142°-145° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04091097
Quelldatensatzuspto-grants-1978_05
ORD IDord-78f9c8f850fa47f8b701f176f07edd1e
Quellennotizuspto-grants-1978_05