関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzenesulfonyl chloride | HCID 7369 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 2(1H)-Quinoxalinone, 3,4-dihydro- | HCID 185949 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 4-(Benzenesulfonyl)-1,3-dihydroquinoxalin-2-one | HCID 1093237 | 52% |
反応手順
A suspension of 10 g. (0.068 mole) of 3,4-dihydro-2(1H)-quinoxalinone (3,4-dihydro-2-hydroxyquinoxaline) [prepared in 50% yield according to the procedure described by W. H. Perkin et al. in the Journal of the Chemical Society, Vol. 123, p.2399(1923)] and 9.6 g. (0.069 mole) of potassium carbonate in 250 ml. of acetone was stirred under a nitrogen atmosphere at 40° C., while 11.5 g. (0.07 mole) of benzenesulfonyl chloride was added during the course of a 30-minute period. The reaction mixture was next heated at reflux temperature for 14 hours and then poured onto 500 ml. of ice. The resulting brown solid was recrystallized from ethyl acetate to yield 10.2 g (52%) of pure 4-benzenesulfonyl-3,4-dihydro-2(1H)-quinoxalinone, m.p. 183°-185° C. The pure product was further characterized by means of nuclear magnetic resonance data and elemental analysis.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04940708 |
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| 出典データセット | uspto-grants-1990_07 |
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| ORD ID | ord-e63bd5bf0967443388cb193dc309b8b9 |
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| 出典メモ | uspto-grants-1990_07 |
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