Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Chlorobenzyl mercaptan | HCID 80409 | — |
| Reactant | 1H-Pyrazole, 3,4,5-trichloro-1-methyl- | HCID 1475184 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 20442317 | HCID 20442317 | — |
Reaction Steps
A stirred mixture of 10.3 g (0.065 moles) 4-chlorobenzyl mercaptan and 3.0 g (0.054 moles) potassium hydroxide in 50 ml dimethylsulfoxide was heated (at about 120° C.) for about 20 minutes. Then 10 g (0.054 moles) 1-methyl-3,4,5-trichloropyrazole were added. Heating (at about 120° C.) of the stirred reaction mixture was continued for about 4 hours. The reaction mixture was allowed to cool. The reaction mixture was added to water (about 50 ml); the resulting mixture was extracted with ether. The etheral phase was separated and dried over magnesium sulfate. The solvent was stripped and the residue was hard-topped. The product was purified by high pressure liquid chromatography to give 6 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04477462 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-28d1fb17d6094691b1ea743a866bcb02 |
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| Source note | uspto-grants-1984_10 |
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