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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459424Generated: October 25, 2026

Iodine → Bis-(2,4-dimethylphenyl)chlorophosphine

https://huagongshe.com/reaction/459424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantBenzene, 1-bromo-2,4-dimethyl-HCID 68503—
ReactantDichloro(diethylamino)phosphineHCID 2733289—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductBis-(2,4-dimethylphenyl)chlorophosphineHCID 11623258—

Reaction Steps

A solution of 2.92 ml (2161 mmol) of 4-bromo-1,3-dimethylbenzene in 3 ml of Et2O were added at 0° C. to a suspension of 0.5 g (20.56 mmol) of magnesium turnings in 7 ml of THF and 7 ml of Et2O and also a crystal of iodine. The mixture was heated to room temperature, stirred further overnight and slowly added dropwise at 0° C. to a solution of 1.5 ml (10.31 mmol) of Et2NPCl2 in 8 ml of THF. The mixture was heated to room temperature and the solvent was subsequently removed under reduced pressure. After adding 60 ml of hexane, the mixture was filtered through Celite under argon and admixed with hydrogen chloride for 1 hour. After degassing, the resulting solids were filtered off under argon and dried. Yield: 1.4 g (58.3% of theory). 1H NMR (400 MHz, CDCl3) δ, 7.40 (d, Jmeta=4.5 Hz, 2H, arom.), 7.2 (m, 4H, arom.), 2.5 (d, JPH=2.0 Hz, 6H, CH3), 2.4 (s, 6H, CH3). 31P NMR (161.974 MHz, CDCl3) δ, 75.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07193092B2
Source datasetuspto-grants-2007_03
ORD IDord-fcafcc4f67fc42058b0d154e0197b24c
Source noteuspto-grants-2007_03