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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 459424Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/459424

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktBenzene, 1-bromo-2,4-dimethyl-HCID 68503—
EduktDichloro(diethylamino)phosphineHCID 2733289—
EduktMagnesiumHCID 5462224—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBis-(2,4-dimethylphenyl)chlorophosphineHCID 11623258—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07193092B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-fcafcc4f67fc42058b0d154e0197b24c
Quellennotizuspto-grants-2007_03