HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3,5-Diiodosalicylic acid → N-[3-chloro-5-methyl-4-[1-(4-chlorophenyl)ethenyl]phenyl]-3,5-diiodo-2-hydroxybenzamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3,5-Diiodosalicylic acid | HCID 8631 | — |
| Edukt | Phosphorus trichloride | HCID 24387 | — |
| Edukt | 1-(4-Amino-2-chloro-6-methylphenyl)-1-(4-chlorophenyl)ethylene | HCID 23323150 | — |
| Produkt | N-[3-chloro-5-methyl-4-[1-(4-chlorophenyl)ethenyl]phenyl]-3,5-diiodo-2-hydroxybenzamide | HCID 23323149 | — |
Reaktionsschritte
Using the reaction sequence of Example 4, 3,5-diiodosalicylic acid is reacted with 1-(4-amino-2-chloro-6-methylphenyl)-1-(4-chlorophenyl)ethylene in the presence of phosphorus trichloride to give N-[3-chloro-5-methyl-4-[1-(4-chlorophenyl)ethenyl]phenyl]-3,5-diiodo-2-hydroxybenzamide. The benzophenone used as starting material for the Wittig reaction was prepared by reacting 4-chlorobenzyl cyanide with 3-chloro-5-methyl-1-nitrobenzene followed by oxidation with alkaline peroxide as known in the literature.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04587361 |
| Quelldatensatz | uspto-grants-1986_05 |
| ORD ID | ord-91459bcd657c4ad9b89aeb1ee04995d5 |
| Quellennotiz | uspto-grants-1986_05 |