KR20000047569A - 플루오로알콜의 제조방법 - Google Patents
플루오로알콜의 제조방법 Download PDFInfo
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- KR20000047569A KR20000047569A KR1019990047371A KR19990047371A KR20000047569A KR 20000047569 A KR20000047569 A KR 20000047569A KR 1019990047371 A KR1019990047371 A KR 1019990047371A KR 19990047371 A KR19990047371 A KR 19990047371A KR 20000047569 A KR20000047569 A KR 20000047569A
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- Prior art keywords
- fluoroalcohol
- preparing
- cfr
- ppm
- free radical
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- AQYSYJUIMQTRMV-UHFFFAOYSA-N hypofluorous acid Chemical compound FO AQYSYJUIMQTRMV-UHFFFAOYSA-N 0.000 title claims abstract description 56
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- 238000000034 method Methods 0.000 title claims description 59
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 63
- 239000000758 substrate Substances 0.000 claims abstract description 21
- 150000003254 radicals Chemical class 0.000 claims abstract description 17
- 238000004821 distillation Methods 0.000 claims abstract description 15
- 239000011541 reaction mixture Substances 0.000 claims abstract description 12
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims abstract description 9
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 claims abstract description 7
- 238000001704 evaporation Methods 0.000 claims description 22
- 230000008020 evaporation Effects 0.000 claims description 22
- 238000006243 chemical reaction Methods 0.000 claims description 19
- 239000002585 base Substances 0.000 claims description 17
- 238000002835 absorbance Methods 0.000 claims description 10
- 229910052731 fluorine Inorganic materials 0.000 claims description 10
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
- -1 alkali metal alkoxide Chemical class 0.000 claims description 9
- 239000003999 initiator Substances 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 6
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical group CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 claims description 5
- 238000010521 absorption reaction Methods 0.000 claims description 4
- KDGNCLDCOVTOCS-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy propan-2-yl carbonate Chemical compound CC(C)OC(=O)OOC(C)(C)C KDGNCLDCOVTOCS-UHFFFAOYSA-N 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 150000002978 peroxides Chemical class 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 239000000975 dye Substances 0.000 description 14
- 239000010410 layer Substances 0.000 description 12
- 239000012535 impurity Substances 0.000 description 9
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000000370 acceptor Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 3
- HUAUNKAZQWMVFY-UHFFFAOYSA-M sodium;oxocalcium;hydroxide Chemical compound [OH-].[Na+].[Ca]=O HUAUNKAZQWMVFY-UHFFFAOYSA-M 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000010926 purge Methods 0.000 description 2
- FVQMJJQUGGVLEP-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOOC(C)(C)C FVQMJJQUGGVLEP-UHFFFAOYSA-N 0.000 description 1
- SZVMZLJAAGWNPG-UHFFFAOYSA-N 1-tert-butylperoxyoctane Chemical compound CCCCCCCCOOC(C)(C)C SZVMZLJAAGWNPG-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- 238000003965 capillary gas chromatography Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001013 indophenol dye Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 239000000434 metal complex dye Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002987 primer (paints) Substances 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- RCOSUMRTSQULBK-UHFFFAOYSA-N sodium;propan-1-olate Chemical compound [Na+].CCC[O-] RCOSUMRTSQULBK-UHFFFAOYSA-N 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C31/34—Halogenated alcohols
- C07C31/38—Halogenated alcohols containing only fluorine as halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/44—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by addition reactions, i.e. reactions involving at least one carbon-to-carbon double or triple bond
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12C—BEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
- C12C11/00—Fermentation processes for beer
- C12C11/02—Pitching yeast
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
- G11B7/244—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
- G11B7/244—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
- G11B7/246—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes
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- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
- G11B7/244—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
- G11B7/246—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes
- G11B7/247—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes methine or polymethine dyes
- G11B7/2472—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes methine or polymethine dyes cyanine
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- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
- G11B7/244—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
- G11B7/246—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes
- G11B7/248—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes porphines; azaporphines, e.g. phthalocyanines
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- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
- G11B7/244—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
- G11B7/249—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing organometallic compounds
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- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/26—Apparatus or processes specially adapted for the manufacture of record carriers
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Optical Record Carriers And Manufacture Thereof (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
Claims (20)
- 메탄올을 유리 라디칼 소스의 존재에서 테트라플루오로에틸렌 또는 헥사플루오로프로필렌과 반응시키는 단계를 포함하며, 상기 반응 혼합물을 염기의 존재에서 증류시키거나 또는 상기 반응 혼합물을 염기와 접촉시킨 후 증류시키는, 다음 일반식 (1)의 플루오로알콜의 제조방법.H(CFR1CF2)nCH2OH (1)(상기에서, R1은 n=1일 때, F 또는 CF3를 나타내고, n=2일 때, F를 나타낸다)
- 제1항에 있어서,상기 염기는 2보다 크지 않은 pKb를 가지는 물질인플루오로알콜의 제조방법.
- 제1항에 있어서,상기 염기는 알칼리 금속 알콕사이드 또는 알칼리 금속 하이드록사이드인플루오로알콜의 제조방법.
- 제1항에 있어서,상기 염기는 나트륨 알콕사이드, 나트륨 하이드록사이드 및 칼륨 하이드록사이드로 구성되는 그룹으로부터 선택되는 최소한 하나인플루오로알콜의 제조방법.
- 제1항에 있어서,증류에 의하여 획득된 일반식 (1)의 플루오로알콜이 50 ppm 보다 크지 않은 증발 잔류물을 가지는플루오로알콜의 제조방법.H(CFR1CF2)nCH2OH (1)(상기에서, R1및 n은 상기에서 정의된 것과 같다)
- 제5항에 있어서,증류에 의하여 획득된 일반식 (1)의 플루오로알콜이 25 ppm 보다 크지 않은 증발 잔류물을 가지는플루오로알콜의 제조방법.H(CFR1CF2)nCH2OH (1)(상기에서, R1및 n은 상기에서 정의된 것과 같다)
- 제5항에 있어서,증류에 의하여 획득된 일반식 (1)의 플루오로알콜이 10 ppm 보다 크지 않은 증발 잔류물을 가지는플루오로알콜의 제조방법.H(CFR1CF2)nCH2OH (1)(상기에서, R1및 n은 상기에서 정의된 것과 같다)
- 제1항에 있어서,상기 유리 라디칼 소스는 반응 개시제, UV 및 열로 구성되는 그룹으로부터 선택되는 최소한 하나인플루오로알콜의 제조방법.
- 제8항에 있어서,상기 유리 라디칼 소스는 반응 온도에서 약 10 시간의 반감기를 가지는 반응 개시제인플루오로알콜의 제조방법.
- 제8항에 있어서,상기 유리 라디칼 소스는 과산화물(peroxide)인플루오로알콜의 제조방법.
- 제8항에 있어서,상기 유리 라디칼 소스는 디-t-부틸퍼옥사이드, t-부틸퍼옥시이소프로필카보네이트 또는 t-부틸퍼옥시-2-에틸헥사노에이트 인플루오로알콜의 제조방법.
- 제1항에 있어서,산 수용체(acid acceptor)가 상기 유리 라디칼 소스와 함께 사용되는플루오로알콜의 제조방법.
- 50 ppm 보다 크지 않은 증발 잔류물을 가지는 다음 일반식 (1)의 플루오로알콜.H(CFR1CF2)nCH2OH (1)(상기에서, R1은 n=1일 때, F 또는 CF3를 나타내고, n=2일 때, F를 나타낸다)
- 제13항에 있어서,상기 증발 잔류물은 25 ppm 보다 크지 않은플루오로알콜.
- 제13항에 있어서,상기 증발 잔류물은 10 ppm 보다 크지 않은플루오로알콜.
- 제13항에 있어서,메탄올에서의 흡수도 (190-300 nm)가 0.2 abs 보다 크지 않은플루오로알콜.
- 제13항에 있어서,메탄올에서의 흡수도 (205 nm)가 0.1 abs 보다 크지 않은플루오로알콜.
- 제17항에 있어서,메탄올에서의 흡소도 (205 nm)가 -0.2 abs 보다 크지 않은플루오로알콜.
- 기판 및 레이저 기록 및/또는 판독을 위하여 적용되는 기판 상의 기록층을 포함하는 정보 기록 매체의 제조를 위한 제13항에 기재된 플루오로알콜의 용도.
- 제1항에 기재된 방법에 의하여 제조되는 다음 일반식 (1)의 플루오로알콜H(CFR1CF2)nCH2OH (1)(상기에서, R1은 n=1일 때, F 또는 CF3를 나타내고, n=2일 때, F를 나타낸다) 또는 제13항에 기재된 다음 일반식 (1)의 플루오로알콜H(CFR1CF2)nCH2OH (1)(상기에서, R1은 n=1일 때, F 또는 CF3를 나타내고, n=2일 때, F를 나타낸다)을 사용하여 제조되는, 기판 및 레이저 기록 및/또는 판독을 위하여 적용되는 기판 상의 기록층을 포함하는 정보 기록 매체.
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JP373972/1998 | 1998-12-28 | ||
JP37397298 | 1998-12-28 | ||
JP48446/1999 | 1999-02-25 | ||
JP11048446A JP3029618B1 (ja) | 1998-12-28 | 1999-02-25 | フッ素アルコ―ルの製造法 |
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KR10-2001-0077064A Division KR100386834B1 (ko) | 1998-12-28 | 2001-12-06 | 플루오로알콜의 제조방법 |
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KR1019990047371A KR100330273B1 (ko) | 1998-12-28 | 1999-10-29 | 플루오로알콜의 제조방법 |
KR10-2001-0077064A KR100386834B1 (ko) | 1998-12-28 | 2001-12-06 | 플루오로알콜의 제조방법 |
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US (1) | US6392105B1 (ko) |
EP (2) | EP0967193B1 (ko) |
JP (1) | JP3029618B1 (ko) |
KR (2) | KR100330273B1 (ko) |
CN (2) | CN1117053C (ko) |
AT (1) | ATE228494T1 (ko) |
AU (1) | AU724446B2 (ko) |
BG (1) | BG103746A (ko) |
BR (1) | BR9904405A (ko) |
CA (1) | CA2282063C (ko) |
DE (1) | DE69904117T2 (ko) |
ES (1) | ES2186286T3 (ko) |
IL (1) | IL131681A0 (ko) |
MX (1) | MXPA99008815A (ko) |
NZ (1) | NZ337609A (ko) |
RU (1) | RU2198160C2 (ko) |
SG (1) | SG76643A1 (ko) |
TW (2) | TWI247733B (ko) |
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US6187969B1 (en) | 1999-03-15 | 2001-02-13 | Daikin Industries, Ltd. | Process for producing fluoroalcohol |
JP3026804B1 (ja) | 1999-03-15 | 2000-03-27 | ダイキン工業株式会社 | フッ素アルコ―ルの製造法 |
EP1073047B1 (en) * | 1999-07-28 | 2006-11-22 | TDK Corporation | Fluorinated alcohol for manufacturing optical recording medium and optical recording medium produced by using the same |
JP4810715B2 (ja) * | 2000-02-25 | 2011-11-09 | ダイキン工業株式会社 | 2,2,3,4,4,4−ヘキサフルオロ−1−ブタノールの製造プロセス及びその用途 |
JP2002069019A (ja) * | 2000-08-28 | 2002-03-08 | Daikin Ind Ltd | 含フッ素アルコールの製造方法 |
JP2002069017A (ja) * | 2000-08-28 | 2002-03-08 | Daikin Ind Ltd | フッ素アルコールの製造方法 |
JP2002069018A (ja) * | 2000-08-28 | 2002-03-08 | Daikin Ind Ltd | 含フッ素アルコールの製造方法 |
US6673976B1 (en) * | 2002-09-19 | 2004-01-06 | Honeywell International, Inc | Process of making fluorinated alcohols |
CN1305825C (zh) * | 2005-03-16 | 2007-03-21 | 中昊晨光化工研究院 | 四氟丙醇的提纯方法 |
US8563115B2 (en) * | 2008-08-12 | 2013-10-22 | Xerox Corporation | Protective coatings for solid inkjet applications |
US8191992B2 (en) * | 2008-12-15 | 2012-06-05 | Xerox Corporation | Protective coatings for solid inkjet applications |
CN102924235B (zh) * | 2012-11-26 | 2016-04-20 | 山东科技大学 | 一种八氟戊醇的提纯方法 |
JP2015193589A (ja) * | 2014-03-26 | 2015-11-05 | セントラル硝子株式会社 | 1,1,1,3,3,3−ヘキサフルオロ−tert−ブタノールの製造方法 |
EP3124479A1 (en) * | 2015-07-29 | 2017-02-01 | Solvay SA | Method for the manufacture of fluorinated cyclic carbonates |
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US2559628A (en) | 1944-04-22 | 1951-07-10 | Du Pont | Fluorine-containing alcohols and process for preparing the same |
JPS54154707A (en) * | 1978-04-21 | 1979-12-06 | Daikin Ind Ltd | Telomerization of tetrafluoroethylene |
JPS57154707A (en) * | 1981-11-27 | 1982-09-24 | Nippon Electric Co | Dielectric composition |
CS244792B1 (cs) * | 1985-01-21 | 1986-08-14 | Oldrich Paleta | Způsob výroby fluorovaných alkanolů |
CS268247B1 (cs) * | 1988-02-22 | 1990-03-14 | Odrich Ing Csc Paleta | Způsob výroby hexafluoralkanolů |
IT1226574B (it) * | 1988-08-02 | 1991-01-24 | Ausimont Spa | Processo per la preparazione di composti fluorurati e nuovi prodotti ottenuti. |
JPH02188540A (ja) | 1989-01-13 | 1990-07-24 | Sumitomo Chem Co Ltd | メタノールの精製法 |
DE3915759A1 (de) * | 1989-05-13 | 1990-11-15 | Hoechst Ag | Verfahren zur herstellung von telomeralkoholen |
JPH048585A (ja) | 1990-04-26 | 1992-01-13 | Fuji Photo Film Co Ltd | 情報記録媒体の製造方法 |
JP2934065B2 (ja) | 1991-07-11 | 1999-08-16 | 富士写真フイルム株式会社 | 情報記録媒体および光情報記録方法 |
JP3334721B2 (ja) | 1992-02-17 | 2002-10-15 | 株式会社リコー | 光記録媒体及びその製造方法 |
JPH05258346A (ja) | 1992-03-11 | 1993-10-08 | Canon Inc | 光学的記録媒体及びその製造方法 |
JP3021967B2 (ja) | 1992-06-04 | 2000-03-15 | 住友化学工業株式会社 | アルコールの精製方法 |
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JPH08291091A (ja) | 1995-04-20 | 1996-11-05 | Fuji Photo Film Co Ltd | 回収メタノールの精製方法及び精製メタノール |
US6187969B1 (en) | 1999-03-15 | 2001-02-13 | Daikin Industries, Ltd. | Process for producing fluoroalcohol |
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CA2282063A1 (en) | 2000-06-28 |
MXPA99008815A (es) | 2007-07-02 |
KR20010112910A (ko) | 2001-12-22 |
EP0967193A3 (en) | 2000-04-26 |
TWI247734B (en) | 2006-01-21 |
ES2186286T3 (es) | 2003-05-01 |
JP2000247916A (ja) | 2000-09-12 |
RU2198160C2 (ru) | 2003-02-10 |
AU724446B2 (en) | 2000-09-21 |
US6392105B1 (en) | 2002-05-21 |
IL131681A0 (en) | 2001-03-19 |
KR100330273B1 (ko) | 2002-04-01 |
EP0967193B1 (en) | 2002-11-27 |
CA2282063C (en) | 2003-11-18 |
ATE228494T1 (de) | 2002-12-15 |
CN1600766A (zh) | 2005-03-30 |
NZ337609A (en) | 2000-09-29 |
TWI247733B (en) | 2006-01-21 |
CN1600766B (zh) | 2010-05-26 |
AU4484499A (en) | 2000-06-29 |
DE69904117D1 (de) | 2003-01-09 |
BG103746A (en) | 2001-08-31 |
BR9904405A (pt) | 2000-09-19 |
SG76643A1 (en) | 2000-11-21 |
JP3029618B1 (ja) | 2000-04-04 |
DE69904117T2 (de) | 2003-07-24 |
EP1179521A1 (en) | 2002-02-13 |
CN1117053C (zh) | 2003-08-06 |
KR100386834B1 (ko) | 2003-06-09 |
TW200510285A (en) | 2005-03-16 |
EP0967193A2 (en) | 1999-12-29 |
CN1258669A (zh) | 2000-07-05 |
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