関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Nitric Acid | HCID 944 | — |
| 反応物 | O-Toluidine | HCID 7242 | — |
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | Acetyl nitrate | HCID 11557 | — |
| 反応物 | 4-Fluoro-2-methylaniline | HCID 67982 | — |
| 生成物 | N-(4-fluoro-2-methyl-6-nitrophenyl)acetamide | HCID 54330341 | — |
反応手順
Stirred acetic anhydride, 300 mL, was cooled to about 7° C., and 25.1 grams (0.20 mole) of 4-fluoro-2-methylaniline was added dropwise during a 30 minute period. Upon completion of addition, the reaction mixture was stirred at about 10° C. for an additional 15 minutes. In a separate reaction vessel, acetyl nitrate was prepared by the dropwise addition of 14.9 mL of 90% nitric acid to 30 mL of stirred, cold (0°-15° C.) acetic anhydride during a 15 minute period. The so-prepared acetyl nitrate was cooled to about -5° C., placed in a dropping funnel, and added dropwise during a 30 minute period to the 2-methylaniline solution. Upon completion of addition, the reaction mixture was stirred an additional 5 hours. After this time the reaction mixture was poured into 400 grams of ice. The resultant solid was collected by filtration, washed with water, and dried at 60° C. under vacuum, yielding 23.0 grams of 5-fluoro-2-methylcarbonylamino-3-methylnitrobenzene, mp 167°-172° C. The NMR spectrum was consistent with the proposed structure.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05616718 |
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| 出典データセット | uspto-grants-1997_04 |
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| ORD ID | ord-e3c956dc6aac4315bf1090e7f781f7ff |
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| 出典メモ | uspto-grants-1997_04 |
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