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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578554Generated: October 31, 2026

Methyl Ethyl Ketone → HCID 21559436, compound

https://huagongshe.com/reaction/1578554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantMethanesulfenyl chloride, trifluoro-HCID 67900—
ProductHCID 21559436HCID 21559436—
ProductHCID 21559444HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03937738
Source datasetuspto-grants-1976_02
ORD IDord-99b8e8d4fd9a459cb35f7f0903e56ee4
Source noteuspto-grants-1976_02