Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582500Generated: October 30, 2026

Dimethyl Sulfate → 1,1,1,2,3,4,4,4-Octafluoro-2-methoxy-3-(trifluoromethyl)butane

https://huagongshe.com/reaction/1582500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantPotassium HydroxideHCID 14797—
ReactantPotassium FluorideHCID 522689—
Reactant1,1,1,3,4,4,4-Heptafluoro-3-(trifluoromethyl)butan-2-oneHCID 14175377—
ReactantMethyl-tri(nonyl)azanium;methyl(trioctyl)azanium;tris-decyl(methyl)azanium;trichlorideHCID 16218603—
SolventWaterHCID 962—
SolventDiglymeHCID 8150—
Product1,1,1,2,3,4,4,4-Octafluoro-2-methoxy-3-(trifluoromethyl)butaneHCID 22987398—

Reaction Steps

The title compound was prepared essentially as in Example 3 using anhydrous potassium fluoride (12.8 g, 0.22 mol), anhydrous diethylene glycol dimethyl ether (diglyme, 106 g), methyltrialkyl(C8-C10)ammonium chloride (Adogen™ 464, available from Aldrich Chemical Company, 4 g), CF3COCF(CF3)2 (53.2 g, 0.20 mol, prepared essentially by the procedure of Smith et al., J. Am. Chem. Soc., 84, 4285 (1962)), and dimethyl sulfate (33.9 g, 0.72 mol). Aqueous potassium hydroxide was added to the reaction mixture (approximately 25 g of 50% solution), followed by water (200 mL). The resulting crude product was azeotropically distilled from the reaction mixture. The lower phase of the resulting distillate was separated from the upper phase, was washed with water, was dried over anhydrous sodium sulfate, and was distilled (b.p. 82-83° C.; yield of 45 g). The product identity was confirmed by GCMS and by FTIR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734154B2
Source datasetuspto-grants-2004_05
ORD IDord-04832279cf924409b6c595d42e880ec9
Source noteuspto-grants-2004_05