Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,2-Dichloroethane | HCID 11 | — |
| Edukt | Hydrogen Peroxide | HCID 784 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Fipronil sulfide | HCID 9953940 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | HCID 178510672 | HCID 178510672 | 80,1% |
Reaktionsschritte
3.0 liter of ethylene dichloride & 421.0 gms of 5-amino-3-cyano-1-(2,6-dichloro-4-trifluromethylphenyl)-4-trifluromethylthio pyrazole was charged in a reactor flask with overhead stirring & condenser system. This mass was cooled to a temperature of about 5-10° C. 95.0 gms of H2O2 (50.0% w/w) & 2000.0 gms H2SO4 (85.0% w/w) were simultaneously added over a period of 3-4 hours. The reaction temperature was maintained at 12-15° C. for about 2.0 hours with monitoring of reaction conversion. The reaction mass obtained thereafter was slowly added into 800 ml of chilled water at a temperature of about 10-20° C. over a period of 2.0 hours. This mass was heated to a temperature of about 60-65° C. to separate the aqueous and organic layers. The organic phase was washed with water & then with 5% NaHCO3, followed by water wash, till a neutral pH was obtained. The crude yield of fipronil after removal of solvent was 435.0 gms. The crude fipronil was then crystallized to yield 350.0 gms of fipronil with 95.50% purity.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09029564B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-ed4ad0baa7574e66a9fb9ab6aca5fd11 |
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| Quellennotiz | uspto-grants-2015_05 |
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