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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217420Generated: October 30, 2026

Diethyl Sulfate → HCID 131729763, compound

https://huagongshe.com/reaction/217420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl SulfateHCID 6163—
ReactantPotassium HydroxideHCID 14797—
ReactantBis(perfluorisopropyl) ketoneHCID 69941—
ReactantPotassium FluorideHCID 522689—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 131729763HCID 1317297636.1%

Reaction Conditions

Temperature52 °C

Reaction Steps

302 grams (0.83 mole) of a ketone mixture of 96.0 percent (CF3)2CFC(O)CF(CF3)2 and 4.0 percent CF3CF2CFC(O)CF(CF3)2, 300 mL anhydrous 1,2-dimethoxyethane, 59.5 grams (1.02 mole) potassium fluoride, 11.1 grams Adogen™ 464 phase transfer catalyst, and 174 grams (1.12 mole) diethyl sulfate were combined in a 2 L flask and heated with stirring to 52° C. for 89 hours. At the end of the 89 hours, the flask was cooled to room temperature, and 230 grams of 45 percent potassium hydroxide and 95 grams of water were added. The resulting mixture was distilled azeotropically using a Dean Stark trap, from which the resulting lower fluorochemical phase was separated during the distillation. The fluorochemical phase was washed twice with an equal volume of water and dried over magnesium sulfate. 53.0 grams of material resulted, with a purity of 37.6 percent (CF3)2CFCF(OC2H5)CF(CF3)2 (yield of 6.1 percent; structure confirmed by GCMS).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193397B2
Source datasetuspto-grants-2012_06
ORD IDord-8e6f1323a7564935a3a3b32fa92d8ddd
Source noteuspto-grants-2012_06