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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992167Generated: October 26, 2026

Toluene → 13,13,13,12,12,11,11,10,10,9,9,8,8,7,7,6,6-Heptadecafluoro-3-oxatridecanoic acid-t-butyl ester

https://huagongshe.com/reaction/992167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant1,1,2,2-Tetrahydroperfluoro-1-decanolHCID 69619—
Reactanttert-Butyl bromoacetateHCID 79177—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventPotassium HydroxideHCID 14797—
Product13,13,13,12,12,11,11,10,10,9,9,8,8,7,7,6,6-Heptadecafluoro-3-oxatridecanoic acid-t-butyl esterHCID 22352715—

Reaction Conditions

Temperature0 °C

Reaction Steps

10.51 g (53.9 mmol) of bromoacetic acid-tert-butyl ester is added in drops to a mixture of 10 g (21.55 mmol) of 1H,1H,2H,2H-perfluorodecan-1-ol and 0.73 g (2.15 mmol) of tetrabutylammonium hydrogen sulfate in 100 ml of 60% potassium hydroxide solution/50 ml of toluene while being stirred vigorously at 0° C. It is stirred for 1 hour at 0° C. 200 ml of toluene is added, the aqueous phase is separated and extracted twice with 50 ml of toluene each. The combined organic phases are dried on magnesium sulfate and concentrated by evaporation in a vacuum. The residue is chromatographed on silica gel (mobile solvent: hexane/dichlormethane/acetone=20/10/1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06468502B1
Source datasetuspto-grants-2002_10
ORD IDord-358a9c4b9de84f8795132100f5476ebc
Source noteuspto-grants-2002_10