Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1076095Erstellt: 26. Oktober 2026

Acetaldehyde → 1-(3,3-Diphenylureido)ethylphosphonic acid

https://huagongshe.com/reaction/1076095

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetaldehydeHCID 177—
EduktCarbon DioxideHCID 280—
EduktTriphenyl phosphiteHCID 7540—
Edukt1,1-DiphenylureaHCID 33603—
EduktPhosphiteHCID 107908—
LösungsmittelBenzeneHCID 241—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
Produkt1-(3,3-Diphenylureido)ethylphosphonic acidHCID 21423551—

Reaktionsschritte

Freshly distilled acetaldehyde (0.22 mole) is added during 0.5 hr to a stirred solution of 0.1 mole each of 1,1-diphenylurea and triphenyl phosphite in 130g of benzene at 60°C. The solution is warmed at reflux (65°-70° with Dry Ice-cooled condenser) for 1.25 hr, giving a dark brown solution having a small 31P nmr peak at -126.2 ppm for unreacted phosphite and a large product peak at -18.4 ppm (~1:5 areas). The reaction mixture is stripped to 130°/3mm. The residue is diluted with 200 ml of acetonitrile and 10g of H2O, and this solution is warmed at reflux for 3 hr. Solid that separates during warming is recrystallized from acetic acid-water to give a white solid: mp 186°-187° dec; p31 nmr -21.6 ppm; 1H nmr δ10.0 (s, 2, OH), 7.3 (m, 10, C6H5 ), 5.4 (d of d, 1, J = 9 and 5Hz, NH), 4.1 (m, 1, CH), 1.3 (d of d, 3, J = 16 and 7 Hz, CH3); acidity 2.00 equiv/ mole, pK1 = 2.20, pK2 = 8.62.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03954860
Quelldatensatzuspto-grants-1976_05
ORD IDord-05bd4ff8d0544eceae7fc02c3017323c
Quellennotizuspto-grants-1976_05