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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017101Generated: October 29, 2026

Perfluoro-2-butanone → HCID 131723633, compound

https://huagongshe.com/reaction/1017101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerfluoro-2-butanoneHCID 3429852—
SolventPyridineHCID 1049—
ProductHCID 131723633HCID 131723633—

Reaction Steps

1341 g of sec-butyl acetate was fluorinated using essentially the same procedure as described in U.S. Pat. No. 5,488,142 (Fall et al.). The resulting perfluorinated ester (688 g) was isolated from the reaction mixture by fractionation. The ester was then decomposed according to the method described by Moore in U.S. Pat. No. 5,466,877 wherein the ester was added dropwise to a 1-liter, 3-neck flask equipped with a magnetic stirrer, dry ice condenser and temperature probe containing 0.5 mL of pyridine. The pot temperature was maintained at about −10° C., during which time the conversion to the ketone occurred. The gaseous ketone product was fractionated to give 435 g. of 1,1,1,3,3,4,4,4-octafluoro-butan-2-one, having a boiling point of 0° C., with purity of 99.7% as determined by gas chromatography and mass spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06478979B1
Source datasetuspto-grants-2002_11
ORD IDord-85775ec79dd3493bbc8169cf4d30a400
Source noteuspto-grants-2002_11