참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| 반응물 | 2,2-Dimethyl-3-(2-hydroxyethyl)-chroman | HCID 54564319 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | 2,2-Dimethyl-3-[2-(4-toluenesulfonyloxy)ethyl]-chroman | HCID 54037841 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05112855 |
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| 출처 데이터셋 | uspto-grants-1992_05 |
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| ORD ID | ord-e893a3e9b8c54aa99dcbad8f7f57b568 |
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| 출처 메모 | uspto-grants-1992_05 |
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