참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | 2-(p-Tolyl)hexafluoroisopropanol | HCID 74829 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-Methanesulfonyloxy-2-p-tolyl-1,1,1,3,3,3-hexafluoropropane | HCID 19700273 | 71.4% |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05716756 |
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| 출처 데이터셋 | uspto-grants-1998_02 |
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| ORD ID | ord-bfa83e74d423487693db90f92360767b |
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| 출처 메모 | uspto-grants-1998_02 |
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