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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53418Generated: October 26, 2026

Potassium Hydroxide → 1H-Perfluorohexane

https://huagongshe.com/reaction/53418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-6-iodohexaneHCID 67733—
CatalystTetrabutylammonium BromideHCID 74236—
SolventIsopropanolHCID 3776—
Product1H-PerfluorohexaneHCID 6773091.2%

Reaction Steps

Into a 1 l four-necked flask equipped with a stirrer, a distillation apparatus-equipped reflux condenser, a dropping funnel and a thermometer, 200 cc of isopropyl alcohol, 87.5 g (0.75 mol) of 48% potassium hydroxide and 1 g of tetrabutyl ammonium 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 3 hours. The conversion at that time was 99.9%. A fraction with a boiling point of up to 75° C. was recovered by distillation from the reactor. This recovered liquid was washed five times with 200 g of water, and acetone and isopropyl alcohol were removed. Thus, 146 g of C6F13H having a purity of 99.9%, was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618986
Source datasetuspto-grants-1997_04
ORD IDord-170786d7e07c432a8a0b319eaf4533a6
Source noteuspto-grants-1997_04