참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Aspirin | HCID 2244 | — |
| 반응물 | N,N'-Dicyclohexylurea | HCID 4277 | — |
| 반응물 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 4-Amino-2,6-dimethylphenol | HCID 82668 | — |
| 용매 | Ethylene Glycol | HCID 174 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 2',4-Dihydroxy-3,5-dimethylbenzanilide | HCID 20327558 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04024253 |
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| 출처 데이터셋 | uspto-grants-1977_05 |
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| ORD ID | ord-9b9a470b46fc4381847be282ed897f77 |
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| 출처 메모 | uspto-grants-1977_05 |
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