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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1247700Erstellt: 26. Oktober 2026

Iodine → 2,2-Diphenyl-1-(diphenylphosphino)-1-methylcyclopropane

https://huagongshe.com/reaction/1247700

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktHexaneHCID 8058—
EduktChlorodiphenylphosphineHCID 66180—
Edukt(2-Bromo-1-phenylcyclopropyl)benzeneHCID 282328—
EduktMagnesiumHCID 5462224—
KatalysatorCopper iodideHCID 83717—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2,2-Diphenyl-1-(diphenylphosphino)-1-methylcyclopropaneHCID 2190913050%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

Under a nitrogen atmosphere, 1-bromo-2,2-diphenylcyclopropane (1.44 g, 5.0 mmol) and magnesium (0.134 g, 5.5 mmol) and THF (10 ml) were placed in a reaction flask. Then, a trace amount of iodine was added and the mixture was stirred at 40° C. for 2 hours. After cooling, copper iodide (0.961 g, 5.0 mmol) and chlorodiphenylphosphine (0.90 ml, 5.0 mmol) were added and the resulting mixture was stirred at 40° C. for 20 hours. After cooling to room temperature, hexane (10 ml) was added to the reaction mixture, and crystal separated was then collected by filtration. The crystal was dissolved in toluene, washed with an aqueous 28% ammonia solution and a brine, and dried over anhydrous magnesium sulfate. The solvent was then removed under reduced pressure and the concentrate was recrystallized from a mixture of methanol and toluene to give the title compound (0.98 g, 50%) as white crystal.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07129367B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-3d2a9b07df3147e3a5fcf8e9e22630ad
Quellennotizuspto-grants-2006_10