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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247704Generated: October 25, 2026

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

https://huagongshe.com/reaction/1247704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantLithium BromideHCID 82050—
ReactantDi-tert-butylchlorophosphineHCID 139566—
ReactantMagnesiumHCID 5462224—
Reactant1-Chloro-1-methyl-2,2-diphenylcyclopropaneHCID 12869608—
CatalystCopper iodideHCID 83717—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductDi-tert-butyl(1-methyl-2,2-diphenylcyclopropyl)phosphaneHCID 2190913125.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

Under a nitrogen atmosphere, 1-chloro-1-methyl-2,2-diphenylcyclopropane (2.43 g, 10.0 mmol), magnesium (0.279 g, 11.5 mmol) and THF (10 ml) were placed in a reaction flask, followed by addition of a trace amount of iodine and stirring at 60° C. for 5 hours. After cooling, copper iodide (1.92 g, 10.0 mmol), lithium bromide (0.879 g, 10.1 mmol) and chlorodi-tert-butylphosphine (2.1 ml, 11.0 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% (w/w) aqueous ammonia and a brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to give the title compound (0.89 g, 25%) as white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129367B2
Source datasetuspto-grants-2006_10
ORD IDord-9094c94026fc4014a56e9606ac7fa179
Source noteuspto-grants-2006_10