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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 511214Erstellt: 25. Oktober 2026

Chlorodimethylphosphine → Dimethyl(3-nitrobenzyl)phosphane oxide

https://huagongshe.com/reaction/511214

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorodimethylphosphineHCID 69936—
EduktBenzene, 1-(bromomethyl)-3-nitro-HCID 77568—
EduktSodium ethoxideHCID 2723922—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktDimethyl(3-nitrobenzyl)phosphane oxideHCID 6725632928%

Reaktionsschritte

A solution of chlorodimethylphosphine (250 mg, 2.60 mmol) in THF (0.7 mL) was added dropwise to a stirred suspension of sodium ethoxide (194 mg, 2.85 mmol) in THF (0.8 mL) at 0° C. The resulting mixture was stirred at room temperature for 30 min. then treated with 1-(bromomethyl)-3-nitrobenzene (560 mg, 2.59 mmol). The mixture was then stirred under nitrogen at 100° C. in a sealed tube for 2 h., concentrated in vacuo and the residue purified by chromatography over silica gel eluting with 5% MeOH in dichloromethane to afford 153 mg of dimethyl(3-nitrobenzyl)phosphane oxide (yield: 28%). 1H-NMR (CDCl3, 400 MHz): δ=1.53 (d, J=12.4 Hz, 6 H), 3.27 (d, J=14.0 Hz, 2 H), 7.55 (t, J=7.6 Hz, 1 H), 7.71 (d, J=7.6 Hz, 1 H), 8.11 (d, J=2.0 Hz, 1 H), 8.16 (dd, J=0.8, 7.2 Hz, 1 H). MS (ES+): m/z 214.00 (MH+). HPLC: tR=2.16 min (ZQ3, polar—5 min).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09096624B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-01462e2659b644d098059711fc17343f
Quellennotizuspto-grants-2015_08