関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Carbon Tetrachloride | HCID 5943 | — |
| 反応物 | Benzenesulfonamide | HCID 7370 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Benzenesulfonylbenzisothiazolone | HCID 67877178 | — |
反応手順
31.44 G. (0.2 mole) of benzenesulfonamide was dissolved in 80 ml. of dry pyridine to obtain a clear, straw-colored solution, which was placed in a cold water bath. To this pyridine solution was added the carbon tetrachloride solution produced in Part B above. An exothermic reaction ensued with formation of a white slurry, which was stirred at ambient temperature for 45 minutes and then poured into 600 ml. of 2N hydrochloric acid. The aqueous phase of the resultant mixture was decanted from the lower organic phase, which was cooled in ice water and filtered to remove carbon tetrachloride. The white solid thus obtained was slurried in 600 ml. of hot acetic acid, cooled and filtered to obtain a white solid, which was dried under vacuum to yield 49.7 g. of product having an infra-red spectrum consistent with the expected structure. The ultraviolet spectrum of the product in methanol showed peaks at 202 nm (ε=17,000), 232 nm. (ε=31,000) and 332 nm. (ε=4,000).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05243052 |
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| 出典データセット | uspto-grants-1993_09 |
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| ORD ID | ord-e42ee508cabb475f98ffdb624b16f4b6 |
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| 出典メモ | uspto-grants-1993_09 |
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