HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53416Generated: October 25, 2026
Potassium Hydroxide → 1H-Perfluorohexane
https://huagongshe.com/reaction/53416
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-6-iodohexane | HCID 67733 | — |
| Catalyst | Tetrabutylphosphonium bromide | HCID 76564 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1H-Perfluorohexane | HCID 67730 | 93.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05618986 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-58ac287d8cc14b7892f4b6e9a504f375 |
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| Source note | uspto-grants-1997_04 |
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