JP2020125282A - 含フッ素化合物の製造方法 - Google Patents
含フッ素化合物の製造方法 Download PDFInfo
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- JP2020125282A JP2020125282A JP2019192562A JP2019192562A JP2020125282A JP 2020125282 A JP2020125282 A JP 2020125282A JP 2019192562 A JP2019192562 A JP 2019192562A JP 2019192562 A JP2019192562 A JP 2019192562A JP 2020125282 A JP2020125282 A JP 2020125282A
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- Prior art keywords
- ethyl
- group
- methyl
- fluorine
- bromo
- Prior art date
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- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 title claims abstract description 45
- 229910052731 fluorine Inorganic materials 0.000 title claims abstract description 45
- 239000011737 fluorine Substances 0.000 title claims abstract description 45
- 150000001875 compounds Chemical class 0.000 title claims abstract description 39
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 30
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 24
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 11
- 239000003504 photosensitizing agent Substances 0.000 claims abstract description 11
- 150000001412 amines Chemical class 0.000 claims abstract description 9
- 239000002904 solvent Substances 0.000 claims abstract description 9
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims abstract description 7
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims abstract description 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 5
- -1 acrylic ester Chemical class 0.000 claims description 106
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 22
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 13
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 11
- SEACYXSIPDVVMV-UHFFFAOYSA-L eosin Y Chemical group [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 SEACYXSIPDVVMV-UHFFFAOYSA-L 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 150000002896 organic halogen compounds Chemical class 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- 238000010521 absorption reaction Methods 0.000 claims description 2
- 159000000000 sodium salts Chemical class 0.000 claims description 2
- 150000001336 alkenes Chemical class 0.000 abstract description 10
- 150000001252 acrylic acid derivatives Chemical class 0.000 abstract description 6
- 230000002950 deficient Effects 0.000 abstract description 6
- 238000007259 addition reaction Methods 0.000 abstract description 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 4
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract description 4
- 150000004820 halides Chemical class 0.000 abstract description 3
- 230000001678 irradiating effect Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 31
- 239000000047 product Substances 0.000 description 19
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 16
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
- 238000002360 preparation method Methods 0.000 description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 6
- 238000005160 1H NMR spectroscopy Methods 0.000 description 5
- JRLTTZUODKEYDH-UHFFFAOYSA-N 8-methylquinoline Chemical group C1=CN=C2C(C)=CC=CC2=C1 JRLTTZUODKEYDH-UHFFFAOYSA-N 0.000 description 5
- 238000005481 NMR spectroscopy Methods 0.000 description 5
- 239000012043 crude product Substances 0.000 description 5
- MKLRSRWVGBWOND-UHFFFAOYSA-N ethyl 4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-2-methylnonanoate Chemical compound CCOC(=O)C(C)CC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F MKLRSRWVGBWOND-UHFFFAOYSA-N 0.000 description 5
- UUIQMZJEGPQKFD-UHFFFAOYSA-N n-butyric acid methyl ester Natural products CCCC(=O)OC UUIQMZJEGPQKFD-UHFFFAOYSA-N 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- BULLJMKUVKYZDJ-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-6-iodohexane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)I BULLJMKUVKYZDJ-UHFFFAOYSA-N 0.000 description 4
- JTYRBFORUCBNHJ-UHFFFAOYSA-N 1-bromo-1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)Br JTYRBFORUCBNHJ-UHFFFAOYSA-N 0.000 description 4
- 239000005641 Methyl octanoate Substances 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000004440 column chromatography Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- DIHKMUNUGQVFES-UHFFFAOYSA-N n,n,n',n'-tetraethylethane-1,2-diamine Chemical compound CCN(CC)CCN(CC)CC DIHKMUNUGQVFES-UHFFFAOYSA-N 0.000 description 4
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 3
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 3
- 235000002597 Solanum melongena Nutrition 0.000 description 3
- 244000061458 Solanum melongena Species 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229940017219 methyl propionate Drugs 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- JZRCRCFPVAXHHQ-UHFFFAOYSA-M 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecanoate Chemical compound [O-]C(=O)CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F JZRCRCFPVAXHHQ-UHFFFAOYSA-M 0.000 description 2
- HPJBSCIUOWQAGG-UHFFFAOYSA-N 5-O-ethyl 1-O-methyl 2,2-difluoro-4-iodopentanedioate Chemical compound CCOC(=O)C(CC(C(=O)OC)(F)F)I HPJBSCIUOWQAGG-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- RHDZARKGDBWIMH-UHFFFAOYSA-N C(C(C(=O)O)I)C(C(F)(F)F)(C(F)(F)F)F Chemical compound C(C(C(=O)O)I)C(C(F)(F)F)(C(F)(F)F)F RHDZARKGDBWIMH-UHFFFAOYSA-N 0.000 description 2
- FXZPEPZYPMNZSO-UHFFFAOYSA-N CC(CC(C(F)(F)F)(F)F)(C(=O)O)I Chemical compound CC(CC(C(F)(F)F)(F)F)(C(=O)O)I FXZPEPZYPMNZSO-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 239000005640 Methyl decanoate Substances 0.000 description 2
- XGGZDBXICRXVNL-UHFFFAOYSA-N OC(CC(C(F)(F)F)(C(F)(F)F)F)C(O)=O Chemical compound OC(CC(C(F)(F)F)(C(F)(F)F)F)C(O)=O XGGZDBXICRXVNL-UHFFFAOYSA-N 0.000 description 2
- 125000005396 acrylic acid ester group Chemical group 0.000 description 2
- 239000003905 agrochemical Substances 0.000 description 2
- 239000012300 argon atmosphere Substances 0.000 description 2
- MYVJFXQZJPEAHF-UHFFFAOYSA-N dimethyl 2,2-difluoro-4-iodopentanedioate Chemical compound COC(=O)C(CC(C(=O)OC)(F)F)I MYVJFXQZJPEAHF-UHFFFAOYSA-N 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000012776 electronic material Substances 0.000 description 2
- HGWXXIZVRRTDKT-UHFFFAOYSA-N ethyl 2,2-difluoro-2-iodoacetate Chemical compound CCOC(=O)C(F)(F)I HGWXXIZVRRTDKT-UHFFFAOYSA-N 0.000 description 2
- OBNCKNCVKJNDBV-UHFFFAOYSA-N ethyl butyrate Chemical compound CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- KWXGJTSJUKTDQU-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-8-iodooctane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)I KWXGJTSJUKTDQU-UHFFFAOYSA-N 0.000 description 1
- AHUMDLIBMIYQMU-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7-pentadecafluoro-7-iodoheptane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)I AHUMDLIBMIYQMU-UHFFFAOYSA-N 0.000 description 1
- WNCBRAVUJRPMCO-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-8-methylnonane Chemical compound CC(C)CC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F WNCBRAVUJRPMCO-UHFFFAOYSA-N 0.000 description 1
- KCEJJSGJNCSQFI-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5-undecafluoro-5-iodopentane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)I KCEJJSGJNCSQFI-UHFFFAOYSA-N 0.000 description 1
- PGRFXXCKHGIFSV-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4-nonafluoro-4-iodobutane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)I PGRFXXCKHGIFSV-UHFFFAOYSA-N 0.000 description 1
- XTGYEAXBNRVNQU-UHFFFAOYSA-N 1,1,1,2,2,3,3-heptafluoro-3-iodopropane Chemical compound FC(F)(F)C(F)(F)C(F)(F)I XTGYEAXBNRVNQU-UHFFFAOYSA-N 0.000 description 1
- FBJVLVWUMYWJMY-UHFFFAOYSA-N 1,1,1,2,2,3,4,4,4-nonafluoro-3-iodobutane Chemical compound FC(F)(F)C(F)(F)C(F)(I)C(F)(F)F FBJVLVWUMYWJMY-UHFFFAOYSA-N 0.000 description 1
- BBZVTTKMXRPMHZ-UHFFFAOYSA-N 1,1,1,2,3,3,3-heptafluoro-2-iodopropane Chemical compound FC(F)(F)C(F)(I)C(F)(F)F BBZVTTKMXRPMHZ-UHFFFAOYSA-N 0.000 description 1
- WYRAAMGCHCLHRD-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,5,5,6-undecafluoro-6-iodocyclohexane Chemical compound FC1(F)C(F)(F)C(F)(F)C(F)(I)C(F)(F)C1(F)F WYRAAMGCHCLHRD-UHFFFAOYSA-N 0.000 description 1
- HVMRCTQKKLONBZ-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,5-nonafluoro-5-iodocyclopentane Chemical compound FC1(F)C(F)(F)C(F)(F)C(F)(I)C1(F)F HVMRCTQKKLONBZ-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- USYVEDJTMCGMKN-UHFFFAOYSA-N 1-bromo-1,1,2,2,2-pentafluoroethane Chemical compound FC(F)(F)C(F)(F)Br USYVEDJTMCGMKN-UHFFFAOYSA-N 0.000 description 1
- LANNRYWUUQMNPF-UHFFFAOYSA-N 1-bromo-1,1,2,2,3,3,3-heptafluoropropane Chemical compound FC(F)(F)C(F)(F)C(F)(F)Br LANNRYWUUQMNPF-UHFFFAOYSA-N 0.000 description 1
- CVEIKEYTQKDDQK-UHFFFAOYSA-N 1-bromo-1,1,2,2,3,3,4,4,4-nonafluorobutane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)Br CVEIKEYTQKDDQK-UHFFFAOYSA-N 0.000 description 1
- GUCKQLMUYQSSMF-UHFFFAOYSA-N 1-bromo-1,1,2,2,3,3,4,4,5,5,5-undecafluoropentane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)Br GUCKQLMUYQSSMF-UHFFFAOYSA-N 0.000 description 1
- VPQQZKWYZYVTMU-UHFFFAOYSA-N 1-bromo-1,1,2,2,3,3,4,4,5,5,6,6,7,7,7-pentadecafluoroheptane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)Br VPQQZKWYZYVTMU-UHFFFAOYSA-N 0.000 description 1
- ZAGWQKRFOLDLGQ-UHFFFAOYSA-N 1-bromo-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexane Chemical compound FC1(F)C(F)(F)C(F)(F)C(F)(Br)C(F)(F)C1(F)F ZAGWQKRFOLDLGQ-UHFFFAOYSA-N 0.000 description 1
- QYRCSKHGOOOILI-UHFFFAOYSA-N 1-bromo-1,2,2,3,3,4,4,5,5-nonafluorocyclopentane Chemical compound FC1(F)C(F)(F)C(F)(F)C(F)(Br)C1(F)F QYRCSKHGOOOILI-UHFFFAOYSA-N 0.000 description 1
- DRNDUZRPDGUSKG-UHFFFAOYSA-N 2-(oxolan-2-yl)acetonitrile;hydrate Chemical compound O.N#CCC1CCCO1 DRNDUZRPDGUSKG-UHFFFAOYSA-N 0.000 description 1
- SULCAUVYSILBCB-UHFFFAOYSA-N 2-bromo-1,1,1,2,3,3,3-heptafluoropropane Chemical compound FC(F)(F)C(F)(Br)C(F)(F)F SULCAUVYSILBCB-UHFFFAOYSA-N 0.000 description 1
- GZDMHZSUSHNESP-UHFFFAOYSA-N 2-bromo-1,1,1,2,3,3,4,4,4-nonafluorobutane Chemical compound FC(F)(F)C(F)(F)C(F)(Br)C(F)(F)F GZDMHZSUSHNESP-UHFFFAOYSA-N 0.000 description 1
- AFENDNXGAFYKQO-UHFFFAOYSA-M 2-hydroxybutyrate Chemical compound CCC(O)C([O-])=O AFENDNXGAFYKQO-UHFFFAOYSA-M 0.000 description 1
- UDQCSCVIYSABCC-UHFFFAOYSA-N 4,4,5,5,5-pentafluoro-2-methylpentanoic acid Chemical compound OC(=O)C(C)CC(F)(F)C(F)(F)F UDQCSCVIYSABCC-UHFFFAOYSA-N 0.000 description 1
- KGKNBEHCIIYOEJ-UHFFFAOYSA-N 5-O-ethyl 1-O-methyl 2,2-difluoro-4-hydroxypentanedioate Chemical compound CCOC(=O)C(CC(C(=O)OC)(F)F)O KGKNBEHCIIYOEJ-UHFFFAOYSA-N 0.000 description 1
- YOFOCUPIDNQJAF-UHFFFAOYSA-N BrC(C(F)(F)F)(C(C(C(F)(F)F)(F)F)(F)F)F Chemical compound BrC(C(F)(F)F)(C(C(C(F)(F)F)(F)F)(F)F)F YOFOCUPIDNQJAF-UHFFFAOYSA-N 0.000 description 1
- SCSQOGNYPFHUAK-UHFFFAOYSA-N CC(CC(C(F)(F)F)(F)F)(C(O)=O)O Chemical compound CC(CC(C(F)(F)F)(F)F)(C(O)=O)O SCSQOGNYPFHUAK-UHFFFAOYSA-N 0.000 description 1
- KAZXRYQDIACGBY-UHFFFAOYSA-N COC(=O)CCC(F)(F)C(F)(F)F Chemical compound COC(=O)CCC(F)(F)C(F)(F)F KAZXRYQDIACGBY-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- AQTLYQKIOQKBFB-UHFFFAOYSA-N IC(C(F)(F)F)(C(C(C(F)(F)F)(F)F)(F)F)F Chemical compound IC(C(F)(F)F)(C(C(C(F)(F)F)(F)F)(F)F)F AQTLYQKIOQKBFB-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- BSCNIRCLHVGUEU-UHFFFAOYSA-N OC(CC(C(F)(F)F)(F)F)C(O)=O Chemical compound OC(CC(C(F)(F)F)(F)F)C(O)=O BSCNIRCLHVGUEU-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- RJCQBQGAPKAMLL-UHFFFAOYSA-N bromotrifluoromethane Chemical compound FC(F)(F)Br RJCQBQGAPKAMLL-UHFFFAOYSA-N 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- ULQJCYNTUFXERG-UHFFFAOYSA-N dimethyl 2,2-difluoro-4-hydroxy-4-methylpentanedioate Chemical compound CC(CC(C(=O)OC)(F)F)(C(=O)OC)O ULQJCYNTUFXERG-UHFFFAOYSA-N 0.000 description 1
- LCUMFTDLZUCKSP-UHFFFAOYSA-N dimethyl 2,2-difluoro-4-hydroxypentanedioate Chemical compound COC(=O)C(O)CC(F)(F)C(=O)OC LCUMFTDLZUCKSP-UHFFFAOYSA-N 0.000 description 1
- NHERJAOJDYECLT-UHFFFAOYSA-N dimethyl 2,2-difluoro-4-iodo-4-methylpentanedioate Chemical compound CC(CC(C(=O)OC)(F)F)(C(=O)OC)I NHERJAOJDYECLT-UHFFFAOYSA-N 0.000 description 1
- RAGZEDHHTPQLAI-UHFFFAOYSA-L disodium;2',4',5',7'-tetraiodo-3-oxospiro[2-benzofuran-1,9'-xanthene]-3',6'-diolate Chemical compound [Na+].[Na+].O1C(=O)C2=CC=CC=C2C21C1=CC(I)=C([O-])C(I)=C1OC1=C(I)C([O-])=C(I)C=C21 RAGZEDHHTPQLAI-UHFFFAOYSA-L 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000001813 ethyl (2R)-2-methylbutanoate Substances 0.000 description 1
- IRSJDVYTJUCXRV-UHFFFAOYSA-N ethyl 2-bromo-2,2-difluoroacetate Chemical compound CCOC(=O)C(F)(F)Br IRSJDVYTJUCXRV-UHFFFAOYSA-N 0.000 description 1
- WEUHXJQHTWGZET-UHFFFAOYSA-N ethyl 2-fluoro-2-methylbutanoate Chemical compound CCOC(=O)C(C)(F)CC WEUHXJQHTWGZET-UHFFFAOYSA-N 0.000 description 1
- ONLLXDPBECIJCM-UHFFFAOYSA-N ethyl 2-fluorobutanoate Chemical compound CCOC(=O)C(F)CC ONLLXDPBECIJCM-UHFFFAOYSA-N 0.000 description 1
- QHGFBTYBHKORRS-UHFFFAOYSA-N ethyl 2-hydroxy-2-methylhexanoate Chemical compound CCCCC(C)(O)C(=O)OCC QHGFBTYBHKORRS-UHFFFAOYSA-N 0.000 description 1
- YMLOBGQJWZESAN-UHFFFAOYSA-N ethyl 2-hydroxy-3-(1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexyl)propanoate Chemical compound CCOC(=O)C(CC1(C(C(C(C(C1(F)F)(F)F)(F)F)(F)F)(F)F)F)O YMLOBGQJWZESAN-UHFFFAOYSA-N 0.000 description 1
- DKWMZPWNIUQROK-UHFFFAOYSA-N ethyl 2-hydroxy-3-(1,2,2,3,3,4,4,5,5-nonafluorocyclopentyl)propanoate Chemical compound CCOC(=O)C(CC1(C(C(C(C1(F)F)(F)F)(F)F)(F)F)F)O DKWMZPWNIUQROK-UHFFFAOYSA-N 0.000 description 1
- OCNVZDKHNZUBQB-UHFFFAOYSA-N ethyl 2-hydroxyheptanoate Chemical compound CCCCCC(O)C(=O)OCC OCNVZDKHNZUBQB-UHFFFAOYSA-N 0.000 description 1
- FYSDAOZGLOPJDD-UHFFFAOYSA-N ethyl 2-iodo-2-methylbutanoate Chemical compound CCOC(=O)C(C)(I)CC FYSDAOZGLOPJDD-UHFFFAOYSA-N 0.000 description 1
- CVKHIWSGHLWGMF-UHFFFAOYSA-N ethyl 2-iodo-3-(1,2,2,3,3,4,4,5,5-nonafluorocyclopentyl)propanoate Chemical compound CCOC(=O)C(CC1(C(C(C(C1(F)F)(F)F)(F)F)(F)F)F)I CVKHIWSGHLWGMF-UHFFFAOYSA-N 0.000 description 1
- VSGQCRLZYRSUMT-UHFFFAOYSA-N ethyl 2-iodoheptanoate Chemical compound CCCCCC(C(=O)OCC)I VSGQCRLZYRSUMT-UHFFFAOYSA-N 0.000 description 1
- HCRBXQFHJMCTLF-UHFFFAOYSA-N ethyl 2-methylbutyrate Chemical compound CCOC(=O)C(C)CC HCRBXQFHJMCTLF-UHFFFAOYSA-N 0.000 description 1
- GGJCZSUQNJRNNU-UHFFFAOYSA-N ethyl 2-methylheptanoate Chemical compound CCCCCC(C)C(=O)OCC GGJCZSUQNJRNNU-UHFFFAOYSA-N 0.000 description 1
- FHDFBFNTCRXSRN-UHFFFAOYSA-N ethyl 4,4,5,5,5-pentafluoropentanoate Chemical compound CCOC(=O)CCC(F)(F)C(F)(F)F FHDFBFNTCRXSRN-UHFFFAOYSA-N 0.000 description 1
- CZQIYZIRNWFMOA-UHFFFAOYSA-N ethyl 4,4,5,5,6,6,6-heptafluorohexanoate Chemical compound CCOC(=O)CCC(F)(F)C(F)(F)C(F)(F)F CZQIYZIRNWFMOA-UHFFFAOYSA-N 0.000 description 1
- SVGVTKCTRLEECJ-UHFFFAOYSA-N ethyl 4,5,5,5-tetrafluoro-2-iodo-2-methyl-4-(trifluoromethyl)pentanoate Chemical compound CCOC(=O)C(C)(CC(C(F)(F)F)(C(F)(F)F)F)I SVGVTKCTRLEECJ-UHFFFAOYSA-N 0.000 description 1
- WDAXFOBOLVPGLV-UHFFFAOYSA-N ethyl isobutyrate Chemical compound CCOC(=O)C(C)C WDAXFOBOLVPGLV-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- PDJAZCSYYQODQF-UHFFFAOYSA-N iodine monofluoride Chemical compound IF PDJAZCSYYQODQF-UHFFFAOYSA-N 0.000 description 1
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- IOBCLXSGWMFVQJ-UHFFFAOYSA-N methyl 2-bromo-2,2-difluoroacetate Chemical compound COC(=O)C(F)(F)Br IOBCLXSGWMFVQJ-UHFFFAOYSA-N 0.000 description 1
- NKAYWKXPXYGZBR-UHFFFAOYSA-N methyl 2-fluorobutanoate Chemical compound CCC(F)C(=O)OC NKAYWKXPXYGZBR-UHFFFAOYSA-N 0.000 description 1
- TVGDZFRFTAZVFB-UHFFFAOYSA-N methyl 2-hydroxy-3-(1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexyl)propanoate Chemical compound COC(=O)C(CC1(C(C(C(C(C1(F)F)(F)F)(F)F)(F)F)(F)F)F)O TVGDZFRFTAZVFB-UHFFFAOYSA-N 0.000 description 1
- DAZJUHZLGQEKCI-UHFFFAOYSA-N methyl 2-hydroxy-3-(1,2,2,3,3,4,4,5,5-nonafluorocyclopentyl)propanoate Chemical compound COC(=O)C(CC1(C(C(C(C1(F)F)(F)F)(F)F)(F)F)F)O DAZJUHZLGQEKCI-UHFFFAOYSA-N 0.000 description 1
- DDMCDMDOHABRHD-UHFFFAOYSA-N methyl 2-hydroxybutanoate Chemical compound CCC(O)C(=O)OC DDMCDMDOHABRHD-UHFFFAOYSA-N 0.000 description 1
- ZKBFAXBOTWDLBL-UHFFFAOYSA-N methyl 2-hydroxyheptanoate Chemical compound CCCCCC(O)C(=O)OC ZKBFAXBOTWDLBL-UHFFFAOYSA-N 0.000 description 1
- NBINNYQISJAKHQ-UHFFFAOYSA-N methyl 2-iodo-3-(1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexyl)propanoate Chemical compound COC(=O)C(CC1(C(C(C(C(C1(F)F)(F)F)(F)F)(F)F)(F)F)F)I NBINNYQISJAKHQ-UHFFFAOYSA-N 0.000 description 1
- BMQVVHLZAWQQEZ-UHFFFAOYSA-N methyl 2-iodo-3-(1,2,2,3,3,4,4,5,5-nonafluorocyclopentyl)propanoate Chemical compound COC(=O)C(CC1(C(C(C(C1(F)F)(F)F)(F)F)(F)F)F)I BMQVVHLZAWQQEZ-UHFFFAOYSA-N 0.000 description 1
- PMTZQSNMGVKVNZ-UHFFFAOYSA-N methyl 2-iodoheptanoate Chemical compound CCCCCC(I)C(=O)OC PMTZQSNMGVKVNZ-UHFFFAOYSA-N 0.000 description 1
- KGVPRVBZKYLXFP-UHFFFAOYSA-N methyl 2-methylundecanoate Chemical compound CCCCCCCCCC(C)C(=O)OC KGVPRVBZKYLXFP-UHFFFAOYSA-N 0.000 description 1
- BXNBTCYTNLTFLJ-UHFFFAOYSA-N methyl 4,4,5,5,6,6,6-heptafluoro-2-methylhexanoate Chemical compound COC(=O)C(C)CC(F)(F)C(F)(F)C(F)(F)F BXNBTCYTNLTFLJ-UHFFFAOYSA-N 0.000 description 1
- OUGVLAVHRNOQEV-UHFFFAOYSA-N methyl 4,4,5,5,6,6,6-heptafluorohexanoate Chemical compound COC(=O)CCC(F)(F)C(F)(F)C(F)(F)F OUGVLAVHRNOQEV-UHFFFAOYSA-N 0.000 description 1
- XNPUIKGMNMTLOL-UHFFFAOYSA-N methyl 4,4,5,5,6,6,7,7,7-nonafluoroheptanoate Chemical compound COC(=O)CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)F XNPUIKGMNMTLOL-UHFFFAOYSA-N 0.000 description 1
- FJZBUFLMJMVOSH-UHFFFAOYSA-N methyl 4,5,5,5-tetrafluoro-2-iodo-2-methyl-4-(trifluoromethyl)pentanoate Chemical compound CC(CC(C(F)(F)F)(C(F)(F)F)F)(C(=O)OC)I FJZBUFLMJMVOSH-UHFFFAOYSA-N 0.000 description 1
- AIJBWQXLHUWYME-UHFFFAOYSA-N methyl 5,5,6,6,6-pentafluorohexanoate Chemical compound COC(=O)CCCC(F)(F)C(F)(F)F AIJBWQXLHUWYME-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- UXPOJVLZTPGWFX-UHFFFAOYSA-N pentafluoroethyl iodide Chemical compound FC(F)(F)C(F)(F)I UXPOJVLZTPGWFX-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- WTWWXOGTJWMJHI-UHFFFAOYSA-N perflubron Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)Br WTWWXOGTJWMJHI-UHFFFAOYSA-N 0.000 description 1
- GVKCHTBDSMQENH-UHFFFAOYSA-L phloxine B Chemical compound [Na+].[Na+].[O-]C(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 GVKCHTBDSMQENH-UHFFFAOYSA-L 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- VPAYJEUHKVESSD-UHFFFAOYSA-N trifluoroiodomethane Chemical compound FC(F)(F)I VPAYJEUHKVESSD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/542—Dye sensitized solar cells
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
で表わされるアクリル酸エステル誘導体を、光増感剤及びアミン類存在下、溶媒中、光照射して、下記一般式(2)
R3−X (2)
(式(2)中、R3は、トリフルオロメチル基、ペンタフルオロエチル基、炭素数3〜8の直鎖、分岐若しくは環式のパーフルオロアルキル基、メトキシカルボニルジフルオロメチル基又はエトキシカルボニルジフルオロメチル基を示し、Xは臭素原子又はヨウ素原子を示す)
で表わされる含フッ素有機ハロゲン化合物を反応させることを特徴とする、
下記一般式(3)
で表わされる含フッ素化合物の製造方法を提供する。
で表わされるアクリル酸エステル誘導体を、酸素、光増感剤及びアミン類存在下、溶媒中、光照射して、下記一般式(2)
R3−X (2)
(式(2)中、R3は、トリフルオロメチル基、ペンタフルオロエチル基、炭素数3〜8の直鎖、分岐若しくは環式のパーフルオロアルキル基、メトキシカルボニルジフルオロメチル基又はエトキシカルボニルジフルオロメチル基を示し、Xは臭素原子又はヨウ素原子を示す)
で表わされる含フッ素有機ハロゲン化合物を反応させることを特徴とする、
下記一般式(3)
で表わされる含フッ素化合物の製造方法を提供する。
1H−NMR,19F−NMR,13C−NMR:日本電子(株)製GSX−400スペクトロメーター(JEOL GSX−400 spectrometer)。
HRMS:Thermo Scientific社製Exactive(LC−MS、LCを通さずに測定)。
1H−NMR(400MHz,CDCl3) δ4.29(2H,d,J=27.0Hz),2.74(1H,d,J=49.0Hz),2.51(1H,d,J=53.1Hz),1.51(3H,s),1.31(3H,t,J=7.1Hz)。
19F−NMR(376MHz,CDCl3)δ−81.28(3F,s),−112.49(1F,dd,J=612.6,271.7Hz),−122.24(2F,s),−123.38(2F,s),−124.52(2F,s),−126.64(2F,s)。
1H−NMR(400MHz,CDCl3)δ1.25−1.29(3H,t,J=7.8Hz),1.31−1.32(3H,d,J=6.8Hz),2.01−2.16(2H,m),2.16−2.79(1H,m),2.85−2.93(1H,m),4.15−4.20(2H,q,J=7.2Hz)。
19F−NMR(376MHz,CDCl3)δ−81.31(3F,s),−113.49(2F,dd,J=277.6,606.8Hz),−122.34(2F,s),−123.38(2F,s),−124.21(2F,s),−126.64(2F,s)。
13C−NMR(151MHz,CDCl3)δ14.01,18.33,32.73,33.74−34.02(t,J=21.1Hz),61.04,174.65。
実施例1と同じ反応装置を用い、エオシンY(13.8mg,0.02mmol,0.05equiv.)をエオシンY(2.8mg,0.004mmol,0.01equiv.)に替えた以外、実施例1と同じ操作を行い、目的物の2−ブロモ−4,4,5,5,6,6,7,7,8,8,9,9,9−トリデカフルオロ−2−メチルノナン酸エチル(5)を収率37%、2−位の臭素原子が水素原子に置換した4,4,5,5,6,6,7,7,8,8,9,9,9−トリデカフルオロ−2−メチルノナン酸エチル(6)を収率19%で得た。
実施例3と同じ反応装置を用い、反応時間を1時間より17時間に替えた以外、実施例3と同じ操作を行い、目的物の4,4,5,5,6,6,7,7,8,8,9,9,9−トリデカフルオロ−2−メチルノナン酸エチル(6)を収率62%で得た。
実施例3と同じ反応装置を用い、ジイソプロピルエチルアミン(103.4mg,0.80mmol,2.0equiv.)に替えてトリエチルアミン(81.0mg,0.80mmol,2.0equiv.)に替え、反応時間を17時間とした以外、実施例3と同じ操作を行い、目的物の4,4,5,5,6,6,7,7,8,8,9,9,9−トリデカフルオロ−2−メチルノナン酸エチル(6)を収率54%で得た。
実施例3と同じ反応装置を用い、ジイソプロピルエチルアミン(103.4mg,0.80mmol,2.0equiv.)に替えてN,N,N‘N’−テトラメチルエチレンジアミン(93.0mg,0.80mmol,2.0equiv.)に替え、反応時間を17時間とした以外、実施例3と同じ操作を行い、目的物の4,4,5,5,6,6,7,7,8,8,9,9,9−トリデカフルオロ−2−メチルノナン酸エチル(6)を収率28%で得た。
1H−NMR(400MHz,CDCl3)δ4.39−4.21(2H,m),2.80−2.67(1H,m),2.57−2.44(1H,m),1.27(3H,s),0.90−0.87(3H,m)。
19F−NMR(376MHz,CDCl3)δ−81.31(3F),−109.98−−115.02(2F,dd,J=1462.3Hz,271.7Hz),−121.25(2F),−123.38(2F),−124.52(2F),−126.67(2F)。
13C−NMR(126MHz,CDCl3)δ175.1,71.3,62.7,39.4(t,J=19.8Hz),27.9,13.9。
実施例7と同じ反応装置を用い、ジイソプロピルエチルアミン(51.7mg,0.40mmol,1.0equiv.)に替えてトリエチルアミン(40.8mg,0.40mmol,1.0equiv.)に替えた以外、実施例7と同じ操作を行い、目的物の4,4,5,5,6,6,7,7,8,8,9,9,9−トリデカフルオロ−2−ヨード−2−メチルノナン酸エチル(7)を収率14%で得た。
実施例7と同じ反応装置を用い、ジイソプロピルエチルアミン(51.7mg,0.40mmol,1.0equiv.)に替えてN,N,N´,N´−テトラメチルエチレンジアミン(46.5mg,0.40mmol,1.0equiv.)に替えた以外、実施例7と同じ操作を行い、目的物の4,4,5,5,6,6,7,7,8,8,9,9,9−トリデカフルオロ−2−ヨード−2−メチルノナン酸エチル(7)を収率9%で得た。
実施例7と同じ反応装置を用い、ジイソプロピルエチルアミン(51.7mg,0.40mmol,1.0equiv.)に替えてN,N,N´,N´−テトラエチルエチレンジアミン(68.9mg,0.40mmol,1.0equiv.)に替えた以外、実施例7と同じ操作を行い、目的物の4,4,5,5,6,6,7,7,8,8,9,9,9−トリデカフルオロ−2−ヨード−2−メチルノナン酸エチル(7)を収率10%で得た。
1H−NMR(400MHz,CDCl3)δ4.39−4.21(2H,m),2.80−2.67(1H,m),2.57−2.44(1H,m),1.27(3H,s),0.90−0.87(3H,m)。
19F−NMR(376MHz,CDCl3)δ−81.31(3F),−109.98−−115.02(2F,dd,J=1462.3Hz,271.7Hz),−121.25(2F),−123.38(2F),−124.52(2F),−126.67(2F)。
HRMSの測定では、エチルメタクリレート及びH+付加体として検出され、計算値が451.057884であるのに対して、測定値は451.0580であった。
実施例11と同じ反応装置を用い、窒素置換せずに反応を実施した以外は、実施例11と同じ操作を行い、目的物の4,4,5,5,6,6,7,7,8,8,9,9,9−トリデカフルオロ−2−ヒドロキシ−2−メチルノナン酸エチル(8)(7.13mg、0.016mmol)を得た(収率8%)。
実施例11と同じ反応装置を用い、1−ヨードトリデカフルオロヘキサン(178.4mg,0.40mmol,2.0equiv.)に替えて1−ブロモトリデカフルオロヘキサン(98.2mg,0.40mmol,2.0equiv.)を用いた以外、実施例11と同じ反応操作を行い、目的物の4,4,5,5,6,6,7,7,8,8,9,9,9−トリデカフルオロ−2−ヒドロキシ−2−メチルノナン酸エチル(8)(41.1mg,0.091mmol)を得た(収率46%)。
Claims (5)
- 下記一般式(1)
で表わされるアクリル酸エステル誘導体を、光増感剤及びアミン類存在下、溶媒中、光照射して、下記一般式(2)
R3−X (2)
(式(2)中、R3は、トリフルオロメチル基、ペンタフルオロエチル基、炭素数3〜8の直鎖、分岐若しくは環式のパーフルオロアルキル基、メトキシカルボニルジフルオロメチル基又はエトキシカルボニルジフルオロメチル基を示し、Xは臭素原子又はヨウ素原子を示す)
で表わされる含フッ素有機ハロゲン化合物を反応させることを特徴とする、
下記一般式(3)
で表わされる含フッ素化合物の製造方法。 - 下記一般式(1)
で表わされるアクリル酸エステル誘導体を、酸素、光増感剤及びアミン類存在下、溶媒中、光照射して、下記一般式(2)
R3−X (2)
(式(2)中、R3は、トリフルオロメチル基、ペンタフルオロエチル基、炭素数3〜8の直鎖、分岐若しくは環式のパーフルオロアルキル基、メトキシカルボニルジフルオロメチル基又はエトキシカルボニルジフルオロメチル基を示し、Xは臭素原子又はヨウ素原子を示す)
で表わされる含フッ素有機ハロゲン化合物を反応させることを特徴とする、
下記一般式(3)
で表わされる含フッ素化合物の製造方法。 - 最大吸収波長が350〜600nmを有する光増感剤を使用することを特徴とする、請求項1又は請求項2に記載の含フッ素化合物の製造方法。
- 光増感剤がエオシンY又はそのナトリウム塩であることを特徴とする、請求項1乃至請求項3のいずれか一項に記載の含フッ素化合物の製造方法。
- 光照射条件が、太陽光又は発光ダイオードによることを特徴とする、請求項1乃至請求項4のいずれか一項に記載の含フッ素化合物の製造方法。
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