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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1247701Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1247701

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktHexaneHCID 8058—
Edukt(2-Bromo-1-phenylcyclopropyl)benzeneHCID 282328—
EduktChlorodiisopropylphosphineHCID 538967—
EduktMagnesiumHCID 5462224—
KatalysatorCopper iodideHCID 83717—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2,2-Diphenyl-1-(diisopropylphosphino)-1-methylcyclopropaneHCID 2190913566%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

Under a nitrogen atmosphere, 1-bromo-2,2-diphenylcyclopropane (1.43 g, 5.0 mmol), magnesium (0.133 g, 5.5 mmol) and THF (10 ml) were placed in a reaction flask, followed by addition of a trace amount of iodine and stirring at 40° C. for 1.5 hours. After cooling, copper iodide (0.952 g, 5.0 mmol) and chlorodiisopropylphosphine (0.80 ml, 5.0 mmol) were added and the resulting mixture was stirred at 40° C. for 5 hours, followed by cooling to room temperature. The resulting mixture was diluted with hexane (20 ml) and crystal separated was collected by filtration. The crystal was dissolved in toluene, and the toluene solution was washed with a 28% aqueous ammonia and a brine, and dried over anhydrous magnesium sulfate. Then, the solvent was removed under reduced pressure to give the title compound (1.06 g, 66%) as white crystal.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07129367B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-c365289a83e448169295659bb3949063
Quellennotizuspto-grants-2006_10