関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Salicylaldehyde | HCID 6998 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 2,5-Difluoronitrobenzene | HCID 67767 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-(4-Fluoro-2-nitrophenoxy)benzaldehyde | HCID 22484060 | — |
反応手順
Sodium hydride (1.66 g) was added in portions to a stirred solution of salicylaldehyde (8.06 g) in N,N-dimethylformamide (100 mL) under nitrogen. To the resulting yellow solution was added 2,5-difluoro-1-nitrobenzene (10.0 g) and N,N-dimethylformamide (10 mL). The reaction was heated at 50° C. for 18 hours and evaporated under vacuum. The oily mixture was taken up in chloroform, and washed with 1 M NaOH, water, 1 M HCl, and brine, dried over magnesium sulfate, and evaporated under vacuum to an orange oil. The oil was treated with ethyl ether, cooled in an ice bath, and the precipitated product was collected by filtration to yield the title compound as white crystals. Mp: 94°-95° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05304644 |
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| 出典データセット | uspto-grants-1994_04 |
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| ORD ID | ord-4bc825cd78374e75817ea559babc00f8 |
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| 出典メモ | uspto-grants-1994_04 |
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