関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Vinylidene fluoride | HCID 6369 | — |
| 反応物 | 1,4-Dioxaspiro(4.5)decane | HCID 9093 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| 反応物 | CID 53628100 | HCID 178418400 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 8-(2,2,2-Trifluoroethylidene)-1,4-dioxaspiro[4.5]decane | HCID 21252678 | — |
反応手順
At −100° C., 22 g of 1,1-difluoroethylene were condensed into a solvent mixture of 400 ml of tetrahydrofuran and 100 ml of diethyl ether. Subsequently, 153 ml of a 1.3 molar solution of sec-BuLi were added dropwise to the reaction solution at a temperature between −90° C. and −100° C. Finally, 31.2 g of 1,4-dioxaspiro[4.5]decane were added, the solution was stirred at −100° C. for another 20 minutes and subsequently warmed to 0° C. with stirring. The reaction solution was poured into an aqueous ammonium chloride and extracted with methylene chloride and the combined organic phases were dried over magnesium sulfate and concentrated. The residue was taken up in 400 ml of methylene chloride and, at −70° C., reacted with 32 g (0.2 mol) of DAST, dissolved in 100 ml of methylene chloride. The mixture was then slowly warmed to 0° C. with stirring, and the reaction solution was subsequently poured into an aqueous ammonium chloride. The product was extracted with diethyl ether and the combined organic phases were dried over MgSO4 and concentrated. The residue was chromatographed over silica gel (petroleum ether/ethyl acetate 4:1), to give the title product as a colourless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06197729B1 |
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| 出典データセット | uspto-grants-2001_03 |
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| ORD ID | ord-06c96a7b378a45e7b9a3621bb1afbcb6 |
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| 出典メモ | uspto-grants-2001_03 |
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