HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017101Generated: October 29, 2026
Perfluoro-2-butanone → HCID 131723633, compound
https://huagongshe.com/reaction/1017101
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Perfluoro-2-butanone | HCID 3429852 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 131723633 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06478979B1 |
|---|
| Source dataset | uspto-grants-2002_11 |
|---|
| ORD ID | ord-85775ec79dd3493bbc8169cf4d30a400 |
|---|
| Source note | uspto-grants-2002_11 |
|---|