Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1195633Erstellt: 26. Oktober 2026

Iodine → Tris(2-methoxyethoxymethyl)phosphine

https://huagongshe.com/reaction/1195633

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktTetrahydrofuranHCID 8028—
EduktPhosphorus trichlorideHCID 24387—
Edukt1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
EduktAcetone cardiceHCID 18522661—
Eduktchloride THFHCID 21908598—
KatalysatorMercury dibromideHCID 24612—
ProduktTris(2-methoxyethoxymethyl)phosphineHCID 54193331—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To ground Mg metal (5.2 g, 214 mmol) was added I2 (1 crystal), HgBr2 (10 mg) and 2 ml of a solution of 2-methoxyethoxymethyl chloride (25 g, 201 mmol) in THF (100 ml) at R.T. After 30 sec, the reaction started and was cooled to -30° C. (dry-ice/acetone). The remaining chloride/THF solution was added dropwise at -20° to -10° C. over 2 h. The mixture was stirred at 0° C. for 2h post-addition and cooled to -78° C. The reagent was then treated with PCl3 (2.2 ml, 25.1 mmol) according to General Method I and the final residue was purified by distillation to afford 1.6 (21%) of tris(2-methoxyethoxymethyl)phosphine as a colorless mobile oil (b.p.=150°-160° [email protected] mmHg). 31P-NMR(CDCl3): -42.7. MS(LREI)m/z=299(M+1 ).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05112595
Quelldatensatzuspto-grants-1992_05
ORD IDord-a608e555ca3c45e790ed0ca057610d93
Quellennotizuspto-grants-1992_05