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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1247702Erstellt: 25. Oktober 2026

Iodine → Di-tert-butyl(1-methyl-2,2-diphenylcyclopropyl)phosphane

https://huagongshe.com/reaction/1247702

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktHexaneHCID 8058—
EduktLithium BromideHCID 82050—
EduktDi-tert-butylchlorophosphineHCID 139566—
Edukt(2-Bromo-1-phenylcyclopropyl)benzeneHCID 282328—
EduktMagnesiumHCID 5462224—
KatalysatorCopper iodideHCID 83717—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktDi-tert-butyl(1-methyl-2,2-diphenylcyclopropyl)phosphaneHCID 2190913147%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

Under a nitrogen atmosphere, 1-bromo-2,2-diphenyl-cyclopropane (1.44 g, 5.0 mmol), magnesium (0.134 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 one hour. After cooling, copper iodide (0.962 g, 5.0 mmol), lithium bromide (0.567 g, 6.5 mmol) and chlorodi-tert-butylphosphine (0.95 ml, 5.0 mmol) were added and the resulting mixture was stirred at 60° C. for 3 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. The solvent was then removed under reduced pressure to give the title compound (0.83 g, 47%) as white crystal.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07129367B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-aec168b5a6f641b3bf59928e3e57392e
Quellennotizuspto-grants-2006_10