関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Sulfur Dioxide | HCID 1119 | — |
| 反応物 | Sodium Nitrite | HCID 23668193 | — |
| 反応物 | 2-Amino-6-difluoromethoxy-benzonitrile | HCID 58100765 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-Cyano-3-difluoromethoxyphenylsulfonyl chloride | HCID 58100767 | 91% |
反応手順
2-Amino-6-difluoromethoxy-benzonitrile (6.4 g, 35 mmol) is dissolved in glacial acetic acid (50 ml). Hydrochloric acid (37%, 12.7 g) is added dropwise at ambient temperature. This mixture is cooled to 5° C. and a solution of sodium nitrite (2.5 g, 36.4 mmol) in Water (8 ml) is added dropwise. The reaction mixture is stirred at 0° C. for 1 hour. The resulting diazonium salt solution is added dropwise at ambient temperature to a mixture of glacial acetic acid (100 ml) saturated at ambient temperature with sulfur dioxide and a solution of CuCl2 (2.18 g, 16.2 mmol) in water (5 ml). The resulting mixture is stirred at ambient temperature for 2 hours. The reaction mixture is poured into an ice/water and extracted three times with dichloromethane. The combined organic phases are dried over sodium sulfate and concentrated to give 2-Cyano-3-difluoromethoxy-benzenesulfonyl chloride (8.5 g, 91% yield) which is used without further purification. 1H-NMR (CDCl3, 400 MHz): 8.10 (d, 1H), 7.85 (t, 1H), 7.75 (d, 1H), 6.75 (t, 1H) ppm.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08524896B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-8a94f41c9d4f4fdaa637af0309b079c2 |
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| 出典メモ | uspto-grants-2013_09 |
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