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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 550328Erstellt: 24. Oktober 2026

Methane → 1,1,1-Trifluoro-2-trifluoromethyl-5-vinyloxy-pentan-2-ol

https://huagongshe.com/de/reaction/550328

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethaneHCID 297—
EduktVinyl AcetateHCID 7904—
EduktSodium CarbonateHCID 10340—
Edukt5,5,5-Trifluoro-4-(trifluoromethyl)pentane-1,4-diolHCID 21895362—
KatalysatorHCID 178478077HCID 178478077—
LösungsmittelTolueneHCID 1140—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1,1,1-Trifluoro-2-trifluoromethyl-5-vinyloxy-pentan-2-olHCID 5876380225%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

1,1,1-Trifluoro-2-trifluoromethyl-2,5-pentanediol (11.3 g, 50 mmol), toluene (50 mL), sodium carbonate (10.6 g,100 mmol), chloro-1,5-cyclooctadiene iridium(I) dimer (0.34 g, 0.5 mmol), vinyl acetate(14 mL, 150 mmol) were placed in a dry 250 mL round-bottom flask equipped with a stir bar, condenser, and nitrogen inlet. The reaction mixture was heated to 100° C. and stirred for 3 hours, after which time it was cooled to room temperature. Diethyl ether (50 mL) was added to quench the reaction. After adding charcoal, the mixture was stirred for 1 hr and filtered with Celite 521. Diethyl ether, excess vinyl acetate, and solvent were distilled off under reduced pressure. The degree of the transetherification of the primary diol was found to be 52% by GC. Vacuum distillation (68-70° C., 15 mm Hg) afforded 3.13 g (25%) of colorless liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07947425B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-916deb0365bf4401a69e629fbff88db9
Quellennotizuspto-grants-2011_05