関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| 反応物 | 2,2-Dimethyl-3-(2-hydroxyethyl)-chroman | HCID 54564319 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 2,2-Dimethyl-3-[2-(4-toluenesulfonyloxy)ethyl]-chroman | HCID 54037841 | — |
反応手順
38 g (0.2 mol) of 4-toluenesulfonyl chloride are added at room temperature, while stirring, to a solution of 37.1 g (0.18 mol) of 2,2-dimethyl-3-(2-hydroxyethyl)-chroman in 150 ml of pyridine, the slightly exothermic reaction being maintained at room temperature with an ice bath. The mixture is then stirred for 4 hours at room temperature. The reaction mixture is then poured onto ice-water and extracted with diethyl ether. The combined ethereal phases are washed three times using 150 ml of citric acid solution (5%) each time and three times using 150 ml of water each time, then dried over sodium sulfate and concentrated by evaporation, yielding 59.1 g (89% of the theoretical yield) of 2,2-dimethyl-3-[2-(4-toluenesulfonyloxy)-ethyl]-chroman in the form of a yellow oil which is further used in that form.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04957928 |
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| 出典データセット | uspto-grants-1990_09 |
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| ORD ID | ord-002930fa073f4aac8dd8ce6edd2762c3 |
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| 出典メモ | uspto-grants-1990_09 |
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