Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methanesulfenyl chloride, trifluoro- | HCID 67900 | — |
| Reactant | HCID 19754555 | HCID 19754555 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19754602 | HCID 19754602 | 56.9% |
Reaction Steps
To a solution of 4.8 g (14.91 mmole) of 1-(2,6-dichloro-4-trifluoromethylphenyl)-5-aminoimidazole in 400 ml of methylene chloride was added 1.3 ml (14.91 mmole) of trifluoromethanesulfenyl chloride at 0° C. The mixture was stirred at 0° C. for 4 h and then at RT for 15 h. Water was added and the mixture was partitioned between water and methylene chloride. The organic layer was dried over anhydrous sodium sulfate and the solvent removed. The residue was recrystallized from methylene chloride to give 3.36 g (52.51% yield) of the desired product., mp 134° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05223525 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-29ff528fcd0f4e03b8ba1157d964ed9d |
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| Source note | uspto-grants-1993_06 |
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