Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Reactant | HCID 18929396 | HCID 18929396 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18929425 | HCID 18929425 | — |
Reaction Steps
Dimethyl disulfide (0.14 ml) and 0.2 ml of tert-butyl nitrite were added dropwise to a solution of 0.2 g of 3-amino-4-chloro-5-(2,6-dichloro-4-trifluoromethylphenyl)-1-methylpyrazole (18) in 5 ml of dry methylene chloride with ice cooling. The mixture was stirred at 0° C. for 30 minutes and thereafter poured into water, followed by extraction with chloroform. The organic layer was washed with brine and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue obtained was purified by column chromatography on silica gel, giving 0.2 g of the desired compound in the form of a light brown oil (quantitative yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05739083 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-42af2326231d421e88ac7bb98e2c77c7 |
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| Source note | uspto-grants-1998_04 |
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