関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Catechol | HCID 289 | — |
| 反応物 | 2-Chloro-1,1,1,4,4,4-hexafluoro-2-butene | HCID 9815 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-(2,2,2-Trifluoroethyl)-2-(trifluoromethyl)-1,3-benzodioxole | HCID 53667303 | — |
反応手順
11 g of pyrocatechol were dissolved in 200 ml of dimethylformamide, and 18 g of 45% strength by weight aqueous sodium hydroxide solution were added. 20 g of 2-chloro-1,1,1,4,4,4-hexafluoro-2-butene were added dropwise to the mixture at 75° C. The mixture was subsequently stirred at 75° C. for 30 minutes. It was then poured onto 500 ml of ice-water and extracted with diethyl ether. The organic phase was washed with water, dried with magnesium sulphate and concentrated. Finally, the product was distilled under a high vacuum. The yield was 15 g (=56%), and the boiling point was 60° C. under 10 mbar. The NMR spectra showed the following characteristic absorptions: 19F-NMR: -59.0 and -84.6 ppm. 1H-NMR: 3.02 ppm.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05482956 |
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| 出典データセット | uspto-grants-1996_01 |
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| ORD ID | ord-a032617baf904ac2961376bc37ffd204 |
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| 出典メモ | uspto-grants-1996_01 |
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