HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Ethyl Ketone → HCID 21559436, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Methanesulfenyl chloride, trifluoro- | HCID 67900 | — |
| Product | HCID 21559436 | HCID 21559436 | — |
| Product | HCID 21559444 | HCID 21559444 | — |
Reaction Steps
Using the method of Example 3, 2-butanone was reacted with trifluoromethanesulfenyl chloride. The reaction mixture was distilled, b.p. 30°-72°C/55 to 60 mm. Vapor phase chromatography of the distillate showed two products to be present in major quantities. Fractional distillation gave 3-trifluoromethylthio-2-butanone, b.p. 66°C/62 mm Hg, and 1-trifluoromethylthio-2-butanone, b.p. 85°C/62 mm Hg. These structures were established by spectral and elemental analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03937738 |
| Source dataset | uspto-grants-1976_02 |
| ORD ID | ord-99b8e8d4fd9a459cb35f7f0903e56ee4 |
| Source note | uspto-grants-1976_02 |