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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764986Generated: November 3, 2026

Toluene → HCID 15406176, compound

https://huagongshe.com/reaction/1764986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant1-Hexanol, 3,3,4,4,5,5,6,6,6-nonafluoro-HCID 74883—
Reactanttert-Butyl bromoacetateHCID 79177—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventPotassium HydroxideHCID 14797—
ProductHCID 15406176HCID 15406176—

Reaction Conditions

Temperature0 °C

Reaction Steps

29.54 g (151.5 mmol) of bromoacetic acid-tert-butyl ester is added in drops to a mixture of 20 g (75.73 mmol) of 1H,1H,2H,2H-perfluorohexan-1-ol and 2.57 g (7.57 mmol) of tetrabutylammonium hydrogen sulfate in 300 ml of 60% aqueous potassium hydroxide solution/200 ml of toluene while being stirred vigorously at 0° C. It is stirred for 1 hour at 0° C. 100 ml of toluene is added, the aqueous phase is separated and extracted twice with 50 ml of toluene. 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-215f1c6da231493f906efc545ade8d6f
Source noteuspto-grants-2007_06