HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1076095Erstellt: 26. Oktober 2026
Acetaldehyde → 1-(3,3-Diphenylureido)ethylphosphonic acid
https://huagongshe.com/reaction/1076095
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetaldehyde | HCID 177 | — |
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | Triphenyl phosphite | HCID 7540 | — |
| Edukt | 1,1-Diphenylurea | HCID 33603 | — |
| Edukt | Phosphite | HCID 107908 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 1-(3,3-Diphenylureido)ethylphosphonic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US03954860 |
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| Quelldatensatz | uspto-grants-1976_05 |
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| ORD ID | ord-05bd4ff8d0544eceae7fc02c3017323c |
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| Quellennotiz | uspto-grants-1976_05 |
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