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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8425Erstellt: 23. Oktober 2026

Methyl Benzoate → (Trifluoromethyl)benzene

https://huagongshe.com/de/reaction/8425

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl BenzoateHCID 7150—
Edukt2,2,2-TrifluoroacetophenoneHCID 9905—
EduktIodobenzeneHCID 11575—
EduktHCID 178419081HCID 178419081—
KatalysatorCopper iodideHCID 83717—
Produkt(Trifluoromethyl)benzeneHCID 736826%

Reaktionsschritte

The trifluoromethyl phenyl sulfone/tBuOK trifluoromethylation method can also be applied to other systems. For instance, methyl benzoate can be trifluoromethylated to generate 2,2,2-trifluoroacetophenone in 30% yield at about −50° C. to about −20° C. CF3Cu can be in situ generated with trifluoromethyl phenyl sulfone/tBuOK and copper iodide (CuI), and then further react with iodobenzene at 80° C. for 20 h to give α,α,α-trifluorotoluene in 26% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087789B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-a6ef70945a064cf8aa5b23fae875897f
Quellennotizuspto-grants-2006_08