HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217420Generated: October 30, 2026
Diethyl Sulfate → HCID 131729763, compound
https://huagongshe.com/reaction/217420
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Sulfate | HCID 6163 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Bis(perfluorisopropyl) ketone | HCID 69941 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 131729763 | HCID 131729763 | 6.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193397B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-8e6f1323a7564935a3a3b32fa92d8ddd |
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| Source note | uspto-grants-2012_06 |
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