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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743741Generated: October 30, 2026

Potassium Hydroxide → 1H-Perfluorohexane

https://huagongshe.com/reaction/743741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-6-iodohexaneHCID 67733—
CatalystTetrabutylphosphonium bromideHCID 76564—
SolventMethanolHCID 887—
Product1H-PerfluorohexaneHCID 6773093.1%

Reaction Steps

Into a 1 l four-necked flask equipped with a stirrer, a distillation apparatus-equipped refluxing condenser, a dropping funnel and a thermometer, 200 cc of methanol, 131 g of (1.1 mols) of 48% potassium hydroxide and 3 g of tetrabutylphosphonium bromide were charged. The reactor was heated to bring the internal temperature to 60° C. Then, 223 g (0.5 mol) of C6F13I was dropwise added thereto over a period of one hour. After completion of dropwise addition, heating and refluxing were continued for two hours. The conversion at that time was 97.0%. A fraction with a boiling point of up to 60° C. was recovered by distillation from the reactor. The recovered liquid was washed with 300 g of water to recover the fluorocarbon. Thus, 149 g of C6F13H having a purity of 99.9%, was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05557017
Source datasetuspto-grants-1996_09
ORD IDord-64f8ce8ecf9d4b1eaa27bed5c5ac41e4
Source noteuspto-grants-1996_09