Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 19806678 | HCID 19806678 | — |
| Reactant | HCID 23717576 | HCID 23717576 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 19806696 | HCID 19806696 | — |
Reaction Steps
To a solution of 3-ethoxy-4,5-dichloroisothiazole (19.8 g, 0.10 mol) in DMF (50 ml) under a nitrogen atmosphere was added sodium methanesulfenate (20.4 g, 0.20 mol). The mixture was warmed to 100° C. and stirred for two days. The reaction mixture was then cooled, diluted with diethyl ether, washed with water, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The residue was chromatographed on a silica gel column, eluting with chloroform, to give 7.1 g of the title compound, mp 85°-87° , crystallized from cyclohexane. A by-product, 3-ethoxy-4,5-bis(methylsulfonyl)isothiazole (3.9 g) was also obtained, mp 158°-160° (crystallized from cyclohexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05171860 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-26c8de8e610746339adcc9475d618aed |
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| Source note | uspto-grants-1992_12 |
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