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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247700Generated: October 26, 2026

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

https://huagongshe.com/reaction/1247700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHexaneHCID 8058—
ReactantChlorodiphenylphosphineHCID 66180—
Reactant(2-Bromo-1-phenylcyclopropyl)benzeneHCID 282328—
ReactantMagnesiumHCID 5462224—
CatalystCopper iodideHCID 83717—
SolventTetrahydrofuranHCID 8028—
Product2,2-Diphenyl-1-(diphenylphosphino)-1-methylcyclopropaneHCID 2190913050%

Reaction Conditions

Temperature40 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129367B2
Source datasetuspto-grants-2006_10
ORD IDord-3d2a9b07df3147e3a5fcf8e9e22630ad
Source noteuspto-grants-2006_10