関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 4,5-Dichloro-2-nitroaniline | HCID 81149 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | HCID 23354227 | HCID 23354227 | 79.2% |
反応手順
The procedure of Mitchell and Williams, J. Org. Chem. 44:4733 (1979) was modified to obtain the title compound. A mixture of 4,5-dichloro-2-nitroaniline (1.59 g, 7.68 mmol, Aldrich), DMF (30 mL, dist. at reduced pressure) and NBS (1.51 g, 8.48 mmol, Aldrich) was stirred at room temperature (25° C.) for two days. The dark brown solution was poured into deionized water (200 mL) and allowed to set for 30 minuets. The mixture was filtered and the solids washed with deionized water giving 1.81 g (82.4%) of the crude bromide as a yellow powder. The powder was crystallized from ethanol/water (5:1) giving 1.74 g (79.2%) of the title compound as bright yellow needles, mp. 132°-4° C., pure by 1H NMR. 1H NMR (CDCl3) 6.82 (s, 2H), 8.32 (s, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05597922 |
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| 出典データセット | uspto-grants-1997_01 |
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| ORD ID | ord-1b3f1766b66d430798b8e5264995278d |
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| 出典メモ | uspto-grants-1997_01 |
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