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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54267Erstellt: 25. Oktober 2026

Tributylstannane → 1-Fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene

https://huagongshe.com/reaction/54267

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributylstannaneHCID 5948—
EduktAzobisisobutyronitrileHCID 6547—
Edukt1-Fluoro-1-phenylsulfonyl-3-methyl-3-(4-chlorophenyl)-1-buteneHCID 53860513—
LösungsmittelCyclohexaneHCID 8078—
Produkt1-Fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-buteneHCID 67632345—

Reaktionsschritte

Under a nitrogen atmosphere, a stirring solution of 22.7 grams (0.067 mole) of 1-fluoro-1-phenylsulfonyl-3-methyl-3-(4-chlorophenyl)-1-butene, 42.0 grams (0.14 mole) of tributyltin hydride, and 0.5 gram (catalyst) of azobisisobutyronitrile in 700 mL of cyclohexane is heated at reflux for about three hours. After this time the reaction mixture is cooled to ambient temperature, and 125 mL of silica gel is added. The mixture is concentrated under reduced pressure, and the residue is subjected to column chromatography. The product-containing fractions are combined and concentrated under reduced pressure, yielding 1-fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05622954
Quelldatensatzuspto-grants-1997_04
ORD IDord-beee978054c2486f921e37cce4ee1d7b
Quellennotizuspto-grants-1997_04