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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382124Generated: October 29, 2026

Hexafluoropropylene → HCID 18364359, compound

https://huagongshe.com/reaction/382124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexafluoropropyleneHCID 8302—
ReactantPotassium CarbonateHCID 11430—
ReactantCyclohexanemethanol, 4-[(ethenyloxy)methyl]-HCID 163934—
SolventAcetonitrileHCID 6342—
ProductHCID 18364359HCID 1836435976%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06308001B1
Source datasetuspto-grants-2001_10
ORD IDord-dfda5b09e08148958484a33239cb61cf
Source noteuspto-grants-2001_10