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HRID 372499作成日:2026年10月26日

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

https://huagongshe.com/reaction/372499

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物AspirinHCID 2244—
反応物N,N'-DicyclohexylureaHCID 4277—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物Sodium HydroxideHCID 14798—
反応物4-Amino-2,6-dimethylphenolHCID 82668—
溶媒Ethylene GlycolHCID 174—
溶媒AcetoneHCID 180—
生成物2',4-Dihydroxy-3,5-dimethylbenzanilideHCID 20327558—

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04091097
出典データセットuspto-grants-1978_05
ORD IDord-78f9c8f850fa47f8b701f176f07edd1e
出典メモuspto-grants-1978_05