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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247702Generated: October 25, 2026

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

https://huagongshe.com/reaction/1247702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHexaneHCID 8058—
ReactantLithium BromideHCID 82050—
ReactantDi-tert-butylchlorophosphineHCID 139566—
Reactant(2-Bromo-1-phenylcyclopropyl)benzeneHCID 282328—
ReactantMagnesiumHCID 5462224—
CatalystCopper iodideHCID 83717—
SolventTetrahydrofuranHCID 8028—
ProductDi-tert-butyl(1-methyl-2,2-diphenylcyclopropyl)phosphaneHCID 2190913147%

Reaction Conditions

Temperature40 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129367B2
Source datasetuspto-grants-2006_10
ORD IDord-aec168b5a6f641b3bf59928e3e57392e
Source noteuspto-grants-2006_10