Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzaldehyde | HCID 240 | — |
| Edukt | Triphenyl phosphite | HCID 7540 | — |
| Edukt | N,N-Dimethylsulfamide | HCID 134472 | — |
| Lösungsmittel | Chlorobenzene | HCID 7964 | — |
| Produkt | HCID 21423543 | HCID 21423543 | 36% |
Reaktionsschritte
A mixture of 0.25 mole each of triphenyl phosphite, benzaldehyde, and N,N-dimethylsulfamide in 130g of chlorobenzene is warmed at 115° C. for 1.5 hrs. After the reaction mixture cools to room temperature, 41.0g (36% yield) of crude product is isolated by filtration. It is washed with water and recrystallized from chlorobenzene, giving a white solid: mp 193°-196°; 31P nmr (DMSO-d6) -14.0 ppm(d, J = 28Hz); 1H nmr δ8.8(d of d, 1, J = 2 and 11, NH), 6.8-7.8(m, 15, aryl), 5.2(d of d, 1, J = 10 and 25Hz, CH), 2.4(s, 6, CH3).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04036913 |
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| Quelldatensatz | uspto-grants-1977_07 |
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| ORD ID | ord-0d77e87ae00a4d888e672628fc48cff5 |
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| Quellennotiz | uspto-grants-1977_07 |
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