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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2398278생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/2398278

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물AspirinHCID 2244—
반응물N,N'-DicyclohexylureaHCID 4277—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물Sodium HydroxideHCID 14798—
반응물4-Amino-2,6-dimethylphenolHCID 82668—
용매Ethylene GlycolHCID 174—
용매AcetoneHCID 180—
생성물2',4-Dihydroxy-3,5-dimethylbenzanilideHCID 20327558—

반응 조건

온도0 °C

반응 단계

Acetylsalicyclic 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04024253
출처 데이터셋uspto-grants-1977_05
ORD IDord-9b9a470b46fc4381847be282ed897f77
출처 메모uspto-grants-1977_05