참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Nitric Acid | HCID 944 | — |
| 반응물 | 3-Acetamido-4-methylbenzoic acid | HCID 243432 | — |
| 반응물 | 2-Amino-4-methyl-3,5-dinitrobenzonitrile | HCID 16726789 | — |
| 생성물 | 3-Acetamido-4-methyl-2-nitrobenzoic acid | HCID 243433 | — |
반응 단계
Fuming nitric acid (100 mL, 2.4 mol) is cooled to about 0° C. (ice/acetone/water bath) and 3-(Acetylamino)-4-methylbenzoic Acid (14) (24.567 g, 127.2 mmol) is added in small portions over about 30 minutes, at rate to maintain the internal reaction temperature <5° C. The hetereogeneous reaction mixture is then stirred at about 0° C. for an additional 1 hour. The reaction mixture is then added to ice water (300 mL) and stirred for about 1 hour. The solid obtained is filtered and dried to provide a mixture of 3-N-acetyl-4-methyl-2-nitro benzoic acid (5) and 3-N-acetyl-4-methyl-5-nitro benzoic acid, in ratio of about 78:22 (27.79 g, 92% Combined Yield). A portion of this mixture (23.458 g) is recrystallized from acetic acid (300 mL) to give 3-(Acetylamino)-4-methyl-2-nitrobenzoic Acid (15), as a white solid (15.370 g, 51% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07304084B2 |
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| 출처 데이터셋 | uspto-grants-2007_12 |
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| ORD ID | ord-bbcd564821964a078314caf03b648d3a |
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| 출처 메모 | uspto-grants-2007_12 |
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