HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Toluene → alpha-Cypermethrin 1-Epimeric Mixture
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Cyclopropanecarboxylic acid | HCID 15655 | — |
| Edukt | Cis-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acid | HCID 41507 | — |
| Edukt | O-(p-toluenesulfonyl)-m-phenoxymandelonitrile | HCID 12945136 | — |
| Katalysator | Tetrabutylammonium Bromide | HCID 74236 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | alpha-Cypermethrin 1-Epimeric Mixture | HCID 9801977 | — |
Reaktionsschritte
Cis-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acid (22 g, 0.105 M) was added to a solution of an inorganic base in water (50 ml). Toluene (100 ml), tetra-n-butylammonium bromide (1.6 g, 5 mole % based on the cyclopropane carboxylic acid) and alpha-cyano-3-phenoxybenzyl p-toluenesulphonate (37.9 g, 0.1 M) were added to the stirred mixture which was then heated at 40°-45° C. for 24 hours. The reaction mixture was then treated as in Example 1 to yield cis-alpha-cyano-3-phenoxybenzyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate as a pale amber oil containing less than 1% trans-isomers.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04409150 |
| Quelldatensatz | uspto-grants-1983_10 |
| ORD ID | ord-be7672de8d3b4f8ab12d14aaba57e654 |
| Quellennotiz | uspto-grants-1983_10 |