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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282459Generated: November 1, 2026

Iodine → 1,1-Bis(4-dimethylaminophenyl)-2-(di-t-butylphosphino)propene

https://huagongshe.com/reaction/1282459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantDi-tert-butylchlorophosphineHCID 139566—
ReactantMagnesiumHCID 5462224—
Reactant1,1-Bis(4-dimethylaminophenyl)-2-bromopropeneHCID 18424498—
CatalystCupric ChlorideHCID 24014—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventHeptaneHCID 8900—
Product1,1-Bis(4-dimethylaminophenyl)-2-(di-t-butylphosphino)propeneHCID 1201082820%

Reaction Steps

Into a reactor were introduced 1.44 g (4.00 mmol) of the 1,1-bis(4-dimethylaminophenyl)-2-bromopropene obtained in Example 4 (2), 0.107 g (4.4 mmol) of magnesium, and 11.5 mL of THF under a nitrogen atmosphere. A slight amount of iodine was added to the mixture to ascertain initiation of a reaction. Thereafter, the reaction mixture was refluxed for 2 hours and then cooled. Thereto were added 0.416 g (4.2 mmol) of copper chloride and 0.91 mL (4.4 mmol) of chlorodi-tert-butylphosphine. The reaction mixture was refluxed for 18 hours and then cooled to room temperature. Thereto were added 22.5 mL of heptane and 7.5 mL of diethyl ether. The crystals yielded were taken out by filtration and dissolved in 30 mL of ethyl acetate. The resultant solution was washed with 28% ammonia water and an aqueous sodium chloride solution and then dried with anhydrous magnesium sulfate. Thereafter, the solvent was removed under reduced pressure. The concentrate was recrystallized from ethanol to obtain 0.34 g (20%) of the target compound as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455720B1
Source datasetuspto-grants-2002_09
ORD IDord-96f37795be044bbba9f6fa6009ca3034
Source noteuspto-grants-2002_09