関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | 2-(p-Tolyl)hexafluoroisopropanol | HCID 74829 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-Methanesulfonyloxy-2-p-tolyl-1,1,1,3,3,3-hexafluoropropane | HCID 19700273 | 71.4% |
反応手順
5.16 g (20 mmol) of 1,1,1,3,3,3-hexafluoro-2-p-tolylpropan-2-ol were dissolved in 50 ml of methylene chloride, and 2.8 g (28 mmol) of triethylamine were added. 3.2 g (22 mmol) of methanesulfonyl chloride were added dropwise, while stirring, to the solution cooled to 5° C. After warming up to room temperature, the mixture was allowed to stand overnight. The precipitated salt was filtered off and the organic solution was evaporated down. The subsequent chromatography (silica gel/methylene chloride) gave 4.8 g of 2-methanesulfonyloxy-2-p-tolyl-1,1,1,3,3,3-hexafluoropropane (pale yellow oil).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05716756 |
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| 出典データセット | uspto-grants-1998_02 |
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| ORD ID | ord-bfa83e74d423487693db90f92360767b |
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| 出典メモ | uspto-grants-1998_02 |
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