SU162826A1 - - Google Patents
Info
- Publication number
- SU162826A1 SU162826A1 SU832180A SU832180A SU162826A1 SU 162826 A1 SU162826 A1 SU 162826A1 SU 832180 A SU832180 A SU 832180A SU 832180 A SU832180 A SU 832180A SU 162826 A1 SU162826 A1 SU 162826A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- polyfluorinated
- fluorine
- metal fluorides
- mixture
- aromatic hydrocarbons
- Prior art date
Links
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 229910001515 alkali metal fluoride Inorganic materials 0.000 claims description 4
- 150000001491 aromatic compounds Chemical class 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 125000001153 fluoro group Chemical group F* 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 2
- -1 fluorides metals Chemical class 0.000 claims description 2
- 150000004820 halides Chemical class 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 229910001512 metal fluoride Inorganic materials 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 8
- ONUFSRWQCKNVSL-UHFFFAOYSA-N 1,2,3,4,5-pentafluoro-6-(2,3,4,5,6-pentafluorophenyl)benzene Chemical group FC1=C(F)C(F)=C(F)C(F)=C1C1=C(F)C(F)=C(F)C(F)=C1F ONUFSRWQCKNVSL-UHFFFAOYSA-N 0.000 description 5
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 4
- 235000003270 potassium fluoride Nutrition 0.000 description 4
- 239000011698 potassium fluoride Substances 0.000 description 4
- JDCMOHAFGDQQJX-UHFFFAOYSA-N 1,2,3,4,5,6,7,8-octafluoronaphthalene Chemical compound FC1=C(F)C(F)=C(F)C2=C(F)C(F)=C(F)C(F)=C21 JDCMOHAFGDQQJX-UHFFFAOYSA-N 0.000 description 3
- 238000004817 gas chromatography Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- ZQBFAOFFOQMSGJ-UHFFFAOYSA-N hexafluorobenzene Chemical compound FC1=C(F)C(F)=C(F)C(F)=C1F ZQBFAOFFOQMSGJ-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000000859 sublimation Methods 0.000 description 2
- 230000008022 sublimation Effects 0.000 description 2
- RTNLUFLDZOAXIC-UHFFFAOYSA-N 1,2,3,4,5,6,7,8-octachloronaphthalene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C2=C(Cl)C(Cl)=C(Cl)C(Cl)=C21 RTNLUFLDZOAXIC-UHFFFAOYSA-N 0.000 description 1
- 229910021583 Cobalt(III) fluoride Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- WZJQNLGQTOCWDS-UHFFFAOYSA-K cobalt(iii) fluoride Chemical compound F[Co](F)F WZJQNLGQTOCWDS-UHFFFAOYSA-K 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000001934 cyclohexanes Chemical class 0.000 description 1
- WVIIMZNLDWSIRH-UHFFFAOYSA-N cyclohexylcyclohexane Chemical group C1CCCCC1C1CCCCC1 WVIIMZNLDWSIRH-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
Publications (1)
Publication Number | Publication Date |
---|---|
SU162826A1 true SU162826A1 (en, 2012) |
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2013030A (en) | Production of organic fluorine compounds | |
US2462402A (en) | Fluorinated hydrocarbons | |
US5045634A (en) | Fluorination of haloolefins | |
Henne | The preparation of aliphatic fluorine compounds | |
US2549988A (en) | Manufacture of organic fluorine compounds | |
US3287425A (en) | Fluorinated compounds and their preparation | |
US2560838A (en) | Preparation of fluorine compounds | |
SU162826A1 (en, 2012) | ||
US5347059A (en) | Process for preparing 1,1-dichloro-1,3,3,3-tetra-fluoropropane | |
Haszeldine | 594. The reactions of fluorocarbon radicals. Part II. The reaction of trifluoroiodomethane with acetylene | |
US2533132A (en) | Vapor phase fluorination | |
US2230925A (en) | Preparation of 1, 1, 1-trifluoro-2-chloro-ethane | |
Chambers et al. | Perfluorocarbon fluids as solvent replacements | |
KR0143906B1 (ko) | 촉매 처리된 불화수소화 방법 | |
Belf et al. | 612. Reactions of polyfluoroaryl bromides with cuprous salts in dimethylformamide | |
GB1574684A (en) | M-bromo-benzotrifluorides | |
WO1998055429A1 (en) | Solvents for use in fluorination reactions | |
KR950004888B1 (ko) | 1,1-디클로로테트라플루오로에탄의 제조방법 | |
US2921099A (en) | Process for the preparation of bromochlorofluoroethanes | |
US2533133A (en) | Replacement of hydrogen with fluorine in hydrogen-and halogen-containing organic compounds using lead tetrafluoride | |
McBee et al. | Direct bromination of fluorinated alkanes | |
US2503077A (en) | Perhalogenated ethylcyclopentane | |
Davis et al. | Vapor Phase Bromination of 1, 1-Difluoroethane | |
US3251890A (en) | Production of hexafluorobenzene | |
US2578720A (en) | Fluorination of fused-ring organic compounds with cobalt trifluoride |