HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 861836Erstellt: 25. Oktober 2026
Triethylamine → 2-Methanesulfonyloxy-2-p-tolyl-1,1,1,3,3,3-hexafluoropropane
https://huagongshe.com/reaction/861836
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | 2-(p-Tolyl)hexafluoroisopropanol | HCID 74829 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-Methanesulfonyloxy-2-p-tolyl-1,1,1,3,3,3-hexafluoropropane | HCID 19700273 | 71,4% |
Reaktionsschritte
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).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05716756 |
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| Quelldatensatz | uspto-grants-1998_02 |
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| ORD ID | ord-bfa83e74d423487693db90f92360767b |
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| Quellennotiz | uspto-grants-1998_02 |
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