関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | P-Toluenesulfonamide | HCID 6269 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | Pentaerythritol tribromide | HCID 15206 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 6-Tosyl-2-oxa-6-azaspiro[3.3]heptane | HCID 23319891 | 69.4% |
反応手順
To a solution of KOH (4.98 g, 0.089 mol) and 4-methylbenzenesulfonamide (5.7 g, 0.033 mol) in 90 ml of ethanol, 3-bromo-2,2-bis(bromomethyl)propan-1-ol (9 g, 0.0277 mol) was added at room temperature and the reaction mixture was heated to reflux for 45 h. The solvent was removed by evaporation, 75 ml of 1 M KOH were added and the white suspension was left to stir for another 2 h at room temperature. The mixture was filtered and the white filter cake was rinsed with water until the washing water was neutral. The filter cake was dried under high vacuum to give 4.87 g 6-toluene-4-sulfonyl-2-oxa-6-azaspiro[3.3]heptane (69%) as a white solid. 1H NMR (300 MHz, CDCl3) δ 7.70-7.68 (m, 2H), 7.36-7.34 (m, 2H), 4.58 (s, 4H), 3.90 (s, 4H), 2.45 (s, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08921383B2 |
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| 出典データセット | uspto-grants-2014_12 |
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| ORD ID | ord-18ab945b6bf84d1985df8941b90708f1 |
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| 出典メモ | uspto-grants-2014_12 |
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