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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53414Generated: October 25, 2026

Methanol → 1H-Perfluorohexane

https://huagongshe.com/reaction/53414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantIsopropanolHCID 3776—
ReactantPotassium HydroxideHCID 14797—
Reactant1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-6-iodohexaneHCID 67733—
CatalystHastelloy CHCID 11332432—
SolventWaterHCID 962—
Product1H-PerfluorohexaneHCID 6773092.2%

Reaction Conditions

Temperature55 °C

Reaction Steps

Into a 20 l Hastelloy C autoclave equipped with a stirrer, a reflux condenser, a dropping funnel and a thermometer, 7700 g of methanol, 60 g of isopropyl alcohol and 1980 g (30 mols) of 85% potassium hydroxide were charged. The reactor was heated to bring the internal temperature to 55° C. Then, 4460 g (10 mols) of C6F13I was fed thereto over a period of two hours. While maintaining the reactor at 55° C. stirring was continued for 10 hours. The conversion was more than 99.9%. Then, 3200 g of water was added to dissolve precipitated potassium iodide. The crude reaction solution was separated into two layers, and the fluorocarbon layer (lower layer) was further washed twice with 3200 g of water to obtain 2951 g of C6F13H (purity: 99.9%, 3.9 ppm of C6F13I was detected). In the reactor, no formation of tar was observed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618986
Source datasetuspto-grants-1997_04
ORD IDord-54f8a64d08b74411b846a4c35d500602
Source noteuspto-grants-1997_04