JPS58109451A - パ−フルオロビシクロヘブタン化合物 - Google Patents
パ−フルオロビシクロヘブタン化合物Info
- Publication number
- JPS58109451A JPS58109451A JP56207476A JP20747681A JPS58109451A JP S58109451 A JPS58109451 A JP S58109451A JP 56207476 A JP56207476 A JP 56207476A JP 20747681 A JP20747681 A JP 20747681A JP S58109451 A JPS58109451 A JP S58109451A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- perfluorobicycloheptane
- water
- group
- fluorination
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- -1 Perfluorobicycloheptane compound Chemical class 0.000 title description 6
- 150000001875 compounds Chemical class 0.000 claims description 25
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 5
- 125000002723 alicyclic group Chemical group 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 238000003682 fluorination reaction Methods 0.000 description 6
- 238000005868 electrolysis reaction Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- BWLBGMIXKSTLSX-UHFFFAOYSA-N 2-hydroxyisobutyric acid Chemical compound CC(C)(O)C(O)=O BWLBGMIXKSTLSX-UHFFFAOYSA-N 0.000 description 1
- 101100346154 Caenorhabditis elegans oma-1 gene Proteins 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000700199 Cavia porcellus Species 0.000 description 1
- 241000951471 Citrus junos Species 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 241000567769 Isurus oxyrinchus Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 241000282849 Ruminantia Species 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000003633 blood substitute Substances 0.000 description 1
- 210000001217 buttock Anatomy 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L magnesium sulphate Substances [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 125000005004 perfluoroethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56207476A JPS58109451A (ja) | 1981-12-21 | 1981-12-21 | パ−フルオロビシクロヘブタン化合物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56207476A JPS58109451A (ja) | 1981-12-21 | 1981-12-21 | パ−フルオロビシクロヘブタン化合物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58109451A true JPS58109451A (ja) | 1983-06-29 |
| JPS642580B2 JPS642580B2 (enrdf_load_stackoverflow) | 1989-01-18 |
Family
ID=16540378
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56207476A Granted JPS58109451A (ja) | 1981-12-21 | 1981-12-21 | パ−フルオロビシクロヘブタン化合物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58109451A (enrdf_load_stackoverflow) |
-
1981
- 1981-12-21 JP JP56207476A patent/JPS58109451A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS642580B2 (enrdf_load_stackoverflow) | 1989-01-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2616733C3 (de) | Verfahren zur Herstellung des Di- und Trimeren von Hexafluorpropen | |
| CN106854195A (zh) | 一种高纯度氟代碳酸乙烯酯的制备方法 | |
| JPH08512095A (ja) | ペルフルオロアルカンスルホニルフルオリドの製造方法 | |
| JPS58109451A (ja) | パ−フルオロビシクロヘブタン化合物 | |
| JPS5892680A (ja) | パ−フルオロビシクロ化合物 | |
| US3871975A (en) | Electrolytic process for production of perfluorocyclohexane derivatives | |
| DE600706C (de) | Verfahren zur Herstellung aromatischer, im Kern fluorierter Verbindungen | |
| JPH03169855A (ja) | 過弗化ヘテロ環式化合物の製法及びこの方法で製造された化合物 | |
| DE10021790B4 (de) | Verfahren zur Herstellung von ω-Aminoalkansulfonsäuren und deren Verwendung als Biopuffer | |
| JPS5896061A (ja) | パ−フルオロ環状アミン | |
| JPS59204192A (ja) | パ−フルオロ環式アミン化合物 | |
| JPS5892658A (ja) | パ−フルオロ化合物 | |
| EP0052319A1 (de) | Verfahren zur Herstellung perfluorierter Sulfonsäurefluoride | |
| DE69605218T2 (de) | Verfahren zur Herstellung von fluorierten Sulfonsäureverbindungen | |
| DE899939C (de) | Verfahren zur Herstellung chlorierter oder bromierter Sultone | |
| US1824951A (en) | Process of making alkyl chlorides | |
| JPS6133828B2 (enrdf_load_stackoverflow) | ||
| JPH0251896B2 (enrdf_load_stackoverflow) | ||
| DE668490C (de) | Verfahren zur Herstellung von stickstoff- und schwefelhaltigen Kondensationsprodukten | |
| JPS591485A (ja) | パ−フルオロ環状アミン化合物 | |
| DE499052C (de) | Verfahren zur Herstellung von Sulfonsaeurehalogeniden | |
| Perkin et al. | LXXX.—The synthesis of ααγ-trimethylglutaric acid, of the cis-and trans-modifications of β-hydroxy-ααγ-trimethylglutaric acid, and of ααγ-trimethylglutaconic acid | |
| DE892750C (de) | Verfahren zur Herstellung von Sulfochloriden aromatischer oder aromatisch-heterocyclischer Verbindungen | |
| JPS6335538A (ja) | ペルフルオロアルキルケトンの製法 | |
| JPS595187A (ja) | パ−フルオロ環状アミン化合物 |