HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382124Generated: October 29, 2026
Hexafluoropropylene → HCID 18364359, compound
https://huagongshe.com/reaction/382124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexafluoropropylene | HCID 8302 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Cyclohexanemethanol, 4-[(ethenyloxy)methyl]- | HCID 163934 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 18364359 | HCID 18364359 | 76% |
Reaction Steps
Hexafluoropropene (264 g, 1.76 mol) was added dropwise to a mechanically stirred mixture of 1,4-cyclohexanedimethanol vinyl ether (300 g, 1.76 mol), acetonitrile (600 mL), and K2CO3 (121 g, 0.88 mol), at 0° C. under N2. The reaction flask was placed in an ice bath to moderate the exothermic reaction during the addition of hexafluoropropene. After complete addition of hexafluoropropene, the reaction mixture was stirred for an additional hour at room temperature and filtered. The filtrate was added to 1.5 L water and mixed well. The lower layer formed was separated, washed with water (3×300 mL), and concentrated under reduced pressure (approximately 0.05 mm Hg) to afford 1,1,2,3,3,3-hexafluoro-1-{[4(vinyloxymethyl)cyclohexyl]methoxy}propane(cis/trans mixture) as a colorless liquid (428 g, 76% yield); b.p. 55-60° C./0.05 mm Hg; Refractive Index 1.4145 at 23.7° C.; GC/MS: m/z at 320 for M+; 19F and 1H NMR spectral data are consistent with the structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06308001B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-dfda5b09e08148958484a33239cb61cf |
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| Source note | uspto-grants-2001_10 |
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