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 | 4-Aminophenyl trifluoromethyl sulphone | HCID 136315 | — |
| 反応物 | Sodium Nitrite | HCID 23668193 | — |
| 生成物 | 4-Trifluoromethanesulfonylbenzene-1-sulfonyl chloride | HCID 61728613 | 84% |
反応手順
Under ice-cooling, thionyl chloride (2.7 mL) was added dropwise to water (16 mL) over 30 min. The mixture was stirred at room temperature for 12 hr to give a sulfur dioxide-containing solution. Under ice-cooling, {4-[(trifluoromethyl)sulfonyl]phenyl}amine (2.0 g) was added to concentrated hydrochloric acid (9 mL) and the mixture was stirred. An aqueous solution (3 mL) of sodium nitrite (0.67 g) was added dropwise while maintaining the inside temperature at not higher than 5° C. and the mixture was further stirred for 15 min. The mixture was gradually added at 5° C. to a mixture of the above-mentioned sulfur dioxide-containing solution added with cuprous chloride (10 mg). Under ice-cooling, the mixture was further stirred for 30 min. After stirring, the precipitated product was collected by filtration, washed with water, and dried in the presence of phosphorus pentoxide under reduced pressure at 50° C. to give the title compound (yield 2.3 g, 84%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08048909B2 |
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| 出典データセット | uspto-grants-2011_11 |
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| ORD ID | ord-9fb177a3968d4c4c8c7b7211d278fb97 |
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| 出典メモ | uspto-grants-2011_11 |
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