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HRID 861836Erstellt: 25. Oktober 2026

Triethylamine → 2-Methanesulfonyloxy-2-p-tolyl-1,1,1,3,3,3-hexafluoropropane

https://huagongshe.com/reaction/861836

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt2-(p-Tolyl)hexafluoroisopropanolHCID 74829—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Methanesulfonyloxy-2-p-tolyl-1,1,1,3,3,3-hexafluoropropaneHCID 1970027371,4%

Reaktionsbedingungen

Temperatur5 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05716756
Quelldatensatzuspto-grants-1998_02
ORD IDord-bfa83e74d423487693db90f92360767b
Quellennotizuspto-grants-1998_02