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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919756Generated: October 26, 2026

Water → 4-[1,1,1,3,3,3-Hexafluoro-2-(methoxymethyl)oxypropan-2-yl]-2-propylphenyl 4-bromobutyl ether

https://huagongshe.com/reaction/1919756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,4-DibromobutaneHCID 8056—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(1,1,1,3,3,3-Hexafluoro-2-(methoxymethoxy)propan-2-yl)-2-propylphenolHCID 59201037—
SolventDimethylformamideHCID 6228—
Product4-[1,1,1,3,3,3-Hexafluoro-2-(methoxymethyl)oxypropan-2-yl]-2-propylphenyl 4-bromobutyl etherHCID 5923509571.3%

Reaction Steps

Potassium carbonate (132.4 mg, 0.96 mmol) was added to a mixed solution of 4-[1,1,1,3,3,3-hexafluoro-2-(methoxymethyl)oxypropan-2-yl]-2-propylphenol (221.1 mg, 0.64 mmol) and 1,4-dibromobutane (1.38 g, 6.39 mmol) in N,N-dimethylformamide (20 mL), followed by stirring overnight. Water was added to the reaction solution, followed by extraction with ethyl acetate. Then, the organic layer was washed with saturated saline, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel preparative thin-layer chromatography (hexane:ethyl acetate=10:1) to obtain 219.5 mg of the title compound (yield: 71%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168666B2
Source datasetuspto-grants-2012_05
ORD IDord-087fdb8a78c64322bc24964330821712
Source noteuspto-grants-2012_05