Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 73033826 | HCID 73033826 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | Fipronil sulfide | HCID 9953940 | 73% |
Reaction Steps
A mixture of 1-(2,6-dichloro-4-trifluoromethylphenylhydrazono) 1,2-dicyano-2-trifluoromethylthio ethane (144 mg; 0.34 mmol), prepared according to Example 3, copper (II) chloride (97 mg; 0.71 mmol), and 4 ml of chlorobezene was stirred for 4 hours at 100° C. The solvent was then evaporated under vacuum. The residue was dissolved in CH2CL2 and the solution was washed by an aqueous solution of 1% ammonia in water. The product was dried over sodium sulphate, and solvent was evaporated under reduced pressure. Purification by flash chromatography on silica gel and crystallization from dichloromethane/hexane gave a white solid (105 mg; 73% yield). The product was then recrystallized in a hexane/toluene mixture to provide a light brown powder (93 mg; 65% yield), melting point 163° C. A second recrystallization provided a white powder of the title product with a melting point 165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07323574B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-96cd5a477b2a4823b1a4b9263d3bb262 |
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| Source note | uspto-grants-2008_01 |
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