Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764985Generated: October 25, 2026

Toluene → HCID 22352715, compound

https://huagongshe.com/reaction/1764985

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—
ProductHCID 22352715HCID 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/dichloromethane/acetone=20/10/1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226578B2
Source datasetuspto-grants-2007_06
ORD IDord-c4f4165d5e1f4a9a8af967a130849eec
Source noteuspto-grants-2007_06