JP6704896B2 - 芳香族第一級ジアミンの製造方法 - Google Patents
芳香族第一級ジアミンの製造方法 Download PDFInfo
- Publication number
- JP6704896B2 JP6704896B2 JP2017500926A JP2017500926A JP6704896B2 JP 6704896 B2 JP6704896 B2 JP 6704896B2 JP 2017500926 A JP2017500926 A JP 2017500926A JP 2017500926 A JP2017500926 A JP 2017500926A JP 6704896 B2 JP6704896 B2 JP 6704896B2
- Authority
- JP
- Japan
- Prior art keywords
- reaction
- amine
- ammonia
- aromatic
- aromatic dialdehyde
- 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.)
- Active
Links
- 125000003118 aryl group Chemical group 0.000 title claims description 46
- 238000004519 manufacturing process Methods 0.000 title description 4
- RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical compound NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 title description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 94
- 238000006243 chemical reaction Methods 0.000 claims description 53
- 238000000034 method Methods 0.000 claims description 50
- 229910021529 ammonia Inorganic materials 0.000 claims description 47
- ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 claims description 37
- 150000001412 amines Chemical class 0.000 claims description 32
- 239000003054 catalyst Substances 0.000 claims description 24
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 23
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims description 23
- 239000001257 hydrogen Substances 0.000 claims description 23
- 229910052739 hydrogen Inorganic materials 0.000 claims description 23
- 238000005984 hydrogenation reaction Methods 0.000 claims description 16
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims description 14
- 150000003141 primary amines Chemical class 0.000 claims description 11
- -1 aromatic primary amine Chemical class 0.000 claims description 9
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 claims description 8
- 150000004984 aromatic diamines Chemical class 0.000 claims description 5
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 claims description 4
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 claims description 4
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 claims description 4
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 claims description 4
- 229940100684 pentylamine Drugs 0.000 claims description 4
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims description 4
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 2
- VKLGKDZCKSMSHG-UHFFFAOYSA-N [5-(aminomethyl)furan-2-yl]methanamine Chemical compound NCC1=CC=C(CN)O1 VKLGKDZCKSMSHG-UHFFFAOYSA-N 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 36
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- 238000005576 amination reaction Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 10
- 150000004985 diamines Chemical class 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000007791 liquid phase Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 6
- 238000004817 gas chromatography Methods 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 238000006268 reductive amination reaction Methods 0.000 description 5
- 150000003335 secondary amines Chemical class 0.000 description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
- PXJJKVNIMAZHCB-UHFFFAOYSA-N 2,5-diformylfuran Chemical compound O=CC1=CC=C(C=O)O1 PXJJKVNIMAZHCB-UHFFFAOYSA-N 0.000 description 4
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
- 239000007868 Raney catalyst Substances 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 150000003512 tertiary amines Chemical class 0.000 description 4
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- 229910000564 Raney nickel Inorganic materials 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical group 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- GAGWMWLBYJPFDD-UHFFFAOYSA-N 2-methyloctane-1,8-diamine Chemical compound NCC(C)CCCCCCN GAGWMWLBYJPFDD-UHFFFAOYSA-N 0.000 description 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 125000003172 aldehyde group Chemical group 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- CUFNKYGDVFVPHO-UHFFFAOYSA-N azulene Chemical compound C1=CC=CC2=CC=CC2=C1 CUFNKYGDVFVPHO-UHFFFAOYSA-N 0.000 description 2
- IZALUMVGBVKPJD-UHFFFAOYSA-N benzene-1,3-dicarbaldehyde Chemical compound O=CC1=CC=CC(C=O)=C1 IZALUMVGBVKPJD-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 2
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 2
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-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
- 230000000694 effects Effects 0.000 description 2
- 239000004210 ether based solvent Substances 0.000 description 2
- 125000001072 heteroaryl group Chemical group 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- PQNFLJBBNBOBRQ-UHFFFAOYSA-N indane Chemical compound C1=CC=C2CCCC2=C1 PQNFLJBBNBOBRQ-UHFFFAOYSA-N 0.000 description 2
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 2
- MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- RIWRFSMVIUAEBX-UHFFFAOYSA-N n-methyl-1-phenylmethanamine Chemical compound CNCC1=CC=CC=C1 RIWRFSMVIUAEBX-UHFFFAOYSA-N 0.000 description 2
- OFMZRGPHZODFOD-UHFFFAOYSA-N naphthalene-1,6-dicarbaldehyde Chemical compound O=CC1=CC=CC2=CC(C=O)=CC=C21 OFMZRGPHZODFOD-UHFFFAOYSA-N 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 description 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 1
- PWGJDPKCLMLPJW-UHFFFAOYSA-N 1,8-diaminooctane Chemical compound NCCCCCCCCN PWGJDPKCLMLPJW-UHFFFAOYSA-N 0.000 description 1
- KXSFECAJUBPPFE-UHFFFAOYSA-N 2,2':5',2''-terthiophene Chemical compound C1=CSC(C=2SC(=CC=2)C=2SC=CC=2)=C1 KXSFECAJUBPPFE-UHFFFAOYSA-N 0.000 description 1
- JFJNVIPVOCESGZ-UHFFFAOYSA-N 2,3-dipyridin-2-ylpyridine Chemical compound N1=CC=CC=C1C1=CC=CN=C1C1=CC=CC=N1 JFJNVIPVOCESGZ-UHFFFAOYSA-N 0.000 description 1
- GFUKMNYMTWAPEZ-UHFFFAOYSA-N 2-(2-formylphenyl)-4-phenylbenzaldehyde Chemical compound O=CC1=CC=CC=C1C1=CC(C=2C=CC=CC=2)=CC=C1C=O GFUKMNYMTWAPEZ-UHFFFAOYSA-N 0.000 description 1
- WRATYACTDCYAIU-UHFFFAOYSA-N 2-(2-phenylphenyl)benzene-1,3-dicarbaldehyde Chemical compound O=CC1=CC=CC(C=O)=C1C1=CC=CC=C1C1=CC=CC=C1 WRATYACTDCYAIU-UHFFFAOYSA-N 0.000 description 1
- PPLBZUGHMSZFLA-UHFFFAOYSA-N 2-[4-(2-formylphenyl)phenyl]benzaldehyde Chemical compound O=CC1=CC=CC=C1C1=CC=C(C=2C(=CC=CC=2)C=O)C=C1 PPLBZUGHMSZFLA-UHFFFAOYSA-N 0.000 description 1
- IMLQTJPSRWSDCQ-UHFFFAOYSA-N 2-phenylbenzene-1,3-dicarbaldehyde Chemical compound O=CC1=CC=CC(C=O)=C1C1=CC=CC=C1 IMLQTJPSRWSDCQ-UHFFFAOYSA-N 0.000 description 1
- ZJBWFJBHLGMEKE-UHFFFAOYSA-N 4-(1-formylcyclohexa-2,4-dien-1-yl)-3-phenylbenzaldehyde Chemical compound C1(CC=CC=C1)(C=1C(=CC(=CC=1)C=O)C1=CC=CC=C1)C=O ZJBWFJBHLGMEKE-UHFFFAOYSA-N 0.000 description 1
- FEHLIYXNTWAEBQ-UHFFFAOYSA-N 4-(4-formylphenyl)benzaldehyde Chemical compound C1=CC(C=O)=CC=C1C1=CC=C(C=O)C=C1 FEHLIYXNTWAEBQ-UHFFFAOYSA-N 0.000 description 1
- YGHMZQVOFVDADV-UHFFFAOYSA-N 4-[4-(4-formylphenyl)phenyl]benzaldehyde Chemical compound C1=CC(C=O)=CC=C1C1=CC=C(C=2C=CC(C=O)=CC=2)C=C1 YGHMZQVOFVDADV-UHFFFAOYSA-N 0.000 description 1
- JHPKSRZYUSLRDI-UHFFFAOYSA-N 5-phenylcyclohexa-2,4-diene-1,1-dicarbaldehyde Chemical compound C1=CC(C=O)(C=O)CC(C=2C=CC=CC=2)=C1 JHPKSRZYUSLRDI-UHFFFAOYSA-N 0.000 description 1
- 239000002028 Biomass Substances 0.000 description 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical compound N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- TZTWOBUHCLWLNK-UHFFFAOYSA-N Cirsiumaldehyde Natural products O1C(C=O)=CC=C1COCC1=CC=C(C=O)O1 TZTWOBUHCLWLNK-UHFFFAOYSA-N 0.000 description 1
- BWLUMTFWVZZZND-UHFFFAOYSA-N Dibenzylamine Chemical compound C=1C=CC=CC=1CNCC1=CC=CC=C1 BWLUMTFWVZZZND-UHFFFAOYSA-N 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- LEHOTFFKMJEONL-UHFFFAOYSA-N Uric Acid Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 description 1
- TVWHNULVHGKJHS-UHFFFAOYSA-N Uric acid Natural products N1C(=O)NC(=O)C2NC(=O)NC21 TVWHNULVHGKJHS-UHFFFAOYSA-N 0.000 description 1
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 1
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- XEXIPRQHXNUUAA-UHFFFAOYSA-N [5-(aminomethyl)oxolan-2-yl]methanamine Chemical compound NCC1CCC(CN)O1 XEXIPRQHXNUUAA-UHFFFAOYSA-N 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 description 1
- 125000005213 alkyl heteroaryl group Chemical group 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- MVCFMBZIWGNJTK-UHFFFAOYSA-N anthracene-1,10-dicarbaldehyde Chemical compound C1=CC=C2C=C3C(C=O)=CC=CC3=C(C=O)C2=C1 MVCFMBZIWGNJTK-UHFFFAOYSA-N 0.000 description 1
- SESSRFZDDUZRQV-UHFFFAOYSA-N anthracene-1,2-dicarbaldehyde Chemical compound C1=CC=CC2=CC3=C(C=O)C(C=O)=CC=C3C=C21 SESSRFZDDUZRQV-UHFFFAOYSA-N 0.000 description 1
- ZVEIMOAZWKSSKF-UHFFFAOYSA-N anthracene-1,4-dicarbaldehyde Chemical compound C1=CC=C2C=C3C(C=O)=CC=C(C=O)C3=CC2=C1 ZVEIMOAZWKSSKF-UHFFFAOYSA-N 0.000 description 1
- VQNPHNBVWOBXAX-UHFFFAOYSA-N anthracene-1,6-dicarbaldehyde Chemical compound C1(=CC=CC2=CC3=CC(=CC=C3C=C12)C=O)C=O VQNPHNBVWOBXAX-UHFFFAOYSA-N 0.000 description 1
- LRKFPBBQGMNLTM-UHFFFAOYSA-N anthracene-1,9-dicarbaldehyde Chemical compound C1=CC=C2C(C=O)=C3C(C=O)=CC=CC3=CC2=C1 LRKFPBBQGMNLTM-UHFFFAOYSA-N 0.000 description 1
- HTKKRNQMBYGFMV-UHFFFAOYSA-N anthracene-2,3-dialdehyde Chemical compound C1=CC=C2C=C(C=C(C(C=O)=C3)C=O)C3=CC2=C1 HTKKRNQMBYGFMV-UHFFFAOYSA-N 0.000 description 1
- HYIHKDGNGMOTMK-UHFFFAOYSA-N anthracene-2,7-dicarbaldehyde Chemical compound C1=C(C=CC2=CC3=CC=C(C=C3C=C12)C=O)C=O HYIHKDGNGMOTMK-UHFFFAOYSA-N 0.000 description 1
- SBRUFOSORMQHES-UHFFFAOYSA-N anthracene-9,10-dialdehyde Chemical compound C1=CC=C2C(C=O)=C(C=CC=C3)C3=C(C=O)C2=C1 SBRUFOSORMQHES-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- YAVVGPBYBUYPSR-UHFFFAOYSA-N benzene;oxygen Chemical compound [O].C1=CC=CC=C1 YAVVGPBYBUYPSR-UHFFFAOYSA-N 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- HHNHBFLGXIUXCM-GFCCVEGCSA-N cyclohexylbenzene Chemical compound [CH]1CCCC[C@@H]1C1=CC=CC=C1 HHNHBFLGXIUXCM-GFCCVEGCSA-N 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical compound N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 description 1
- 229910000071 diazene Inorganic materials 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 1
- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- GFAUNYMRSKVDJL-UHFFFAOYSA-N formyl chloride Chemical compound ClC=O GFAUNYMRSKVDJL-UHFFFAOYSA-N 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 150000002485 inorganic esters Chemical class 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- FRQONEWDWWHIPM-UHFFFAOYSA-N n,n-dicyclohexylcyclohexanamine Chemical compound C1CCCCC1N(C1CCCCC1)C1CCCCC1 FRQONEWDWWHIPM-UHFFFAOYSA-N 0.000 description 1
- WYZDCUGWXKHESN-UHFFFAOYSA-N n-benzyl-n-methyl-1-phenylmethanamine Chemical compound C=1C=CC=CC=1CN(C)CC1=CC=CC=C1 WYZDCUGWXKHESN-UHFFFAOYSA-N 0.000 description 1
- DYUWTXWIYMHBQS-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine Chemical compound C=CCNCC=C DYUWTXWIYMHBQS-UHFFFAOYSA-N 0.000 description 1
- WMPJPAMWRAOQSU-UHFFFAOYSA-N naphthalene-1,2-dicarbaldehyde Chemical compound C1=CC=CC2=C(C=O)C(C=O)=CC=C21 WMPJPAMWRAOQSU-UHFFFAOYSA-N 0.000 description 1
- MKCWDCITCTYJFW-UHFFFAOYSA-N naphthalene-1,3-dicarbaldehyde Chemical compound C1=CC=CC2=CC(C=O)=CC(C=O)=C21 MKCWDCITCTYJFW-UHFFFAOYSA-N 0.000 description 1
- YAELIZGEEWGECG-UHFFFAOYSA-N naphthalene-1,5-dicarbaldehyde Chemical compound C1=CC=C2C(C=O)=CC=CC2=C1C=O YAELIZGEEWGECG-UHFFFAOYSA-N 0.000 description 1
- OLSDXRNBPWAEDJ-UHFFFAOYSA-N naphthalene-1,7-dicarbaldehyde Chemical compound C1=CC=C(C=O)C2=CC(C=O)=CC=C21 OLSDXRNBPWAEDJ-UHFFFAOYSA-N 0.000 description 1
- PYHRFGZORIHOMQ-UHFFFAOYSA-N naphthalene-1,8-dicarbaldehyde Chemical compound C1=CC(C=O)=C2C(C=O)=CC=CC2=C1 PYHRFGZORIHOMQ-UHFFFAOYSA-N 0.000 description 1
- IQDQMRZGMILNMQ-UHFFFAOYSA-N naphthalene-2,6-dicarbaldehyde Chemical compound C1=C(C=O)C=CC2=CC(C=O)=CC=C21 IQDQMRZGMILNMQ-UHFFFAOYSA-N 0.000 description 1
- 229910000484 niobium oxide Inorganic materials 0.000 description 1
- URLJKFSTXLNXLG-UHFFFAOYSA-N niobium(5+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Nb+5].[Nb+5] URLJKFSTXLNXLG-UHFFFAOYSA-N 0.000 description 1
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229930184652 p-Terphenyl Natural products 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- RKPUJZVCCNLCAG-UHFFFAOYSA-N phenanthrene-1,2-dicarbaldehyde Chemical compound C1=CC=C2C3=CC=C(C=O)C(C=O)=C3C=CC2=C1 RKPUJZVCCNLCAG-UHFFFAOYSA-N 0.000 description 1
- CKHBAYYUUINPAA-UHFFFAOYSA-N phenanthrene-1,4-dicarbaldehyde Chemical compound C1(=CC=C(C=2C3=CC=CC=C3C=CC1=2)C=O)C=O CKHBAYYUUINPAA-UHFFFAOYSA-N 0.000 description 1
- CXUXWTXQLYNIGZ-UHFFFAOYSA-N phenanthrene-1,9-dicarbaldehyde Chemical compound C1(=CC=CC=2C3=CC=CC=C3C(=CC1=2)C=O)C=O CXUXWTXQLYNIGZ-UHFFFAOYSA-N 0.000 description 1
- MQUYNQCLXAXEDJ-UHFFFAOYSA-N phenanthrene-3,5-dicarbaldehyde Chemical compound C1=CC(=CC2=C3C(=CC=CC3=CC=C12)C=O)C=O MQUYNQCLXAXEDJ-UHFFFAOYSA-N 0.000 description 1
- UWQILXSIEKHHDJ-UHFFFAOYSA-N phenanthrene-9,10-dicarbaldehyde Chemical compound C1=CC=C2C(C=O)=C(C=O)C3=CC=CC=C3C2=C1 UWQILXSIEKHHDJ-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- ZWLUXSQADUDCSB-UHFFFAOYSA-N phthalaldehyde Chemical compound O=CC1=CC=CC=C1C=O ZWLUXSQADUDCSB-UHFFFAOYSA-N 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 150000003140 primary amides Chemical class 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- ILVXOBCQQYKLDS-UHFFFAOYSA-N pyridine N-oxide Chemical compound [O-][N+]1=CC=CC=C1 ILVXOBCQQYKLDS-UHFFFAOYSA-N 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000003349 semicarbazides Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
- 229940116269 uric acid Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/52—Radicals substituted by nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/24—Preparation of compounds containing amino groups bound to a carbon skeleton by reductive alkylation of ammonia, amines or compounds having groups reducible to amino groups, with carbonyl compounds
- C07C209/26—Preparation of compounds containing amino groups bound to a carbon skeleton by reductive alkylation of ammonia, amines or compounds having groups reducible to amino groups, with carbonyl compounds by reduction with hydrogen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J25/00—Catalysts of the Raney type
- B01J25/02—Raney nickel
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/26—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
Description
200mgのRaney Coを含有する100mLのパー(Parr)反応器に、2.0ミリモルのDFFおよび6.0ミリモルのN−ブチルアミンを25mLのエタノールと共に導入した。反応器を次に3回窒素でパージし、混合物をアンモニア雰囲気(0.2MPa)下でかき混ぜてアルコール中におおよそ2gのアンモニアを溶解させた。水素を次に反応器へ導入して2MPaの水素分圧を提供し、反応は次に150℃の温度で3時間進行した。反応の完了後に、反応器を冷まし、未反応アンモニアを放出した。ガスクロマトグラフィーによる反応器中の残留液相の分析は、112mgのFDAが得られ、使用されたDFFを基準として44%の収率を与えることを明らかにした。
米国特許第6,696,609号明細書の実施例1を、反応系での第一級アミンの発生を抑えるための同一の実験条件で、この比較例において再現した。
200mgのRaney Coを含有する100mLのParr反応器に、2.0ミリモルのDFFおよび6.0ミリモルのメチルアミン(40重量%水溶液の形態での)を25mLのメタノールと共に導入した。反応器を次に3回窒素でパージし、混合物をアンモニア雰囲気(0.2MPa)下でかき混ぜてアルコール中におおよそ2gのアンモニアを溶解させた。水素を次に反応器へ導入して2MPaの水素分圧を提供し、反応は次に115〜120℃の温度で3時間進行した。反応の完了後に、反応器を冷まし、未反応アンモニアを放出した。ガスクロマトグラフィーによる反応器中の残留液相の分析は、97mgのFDAが得られ、使用されたDFFを基準として33%の収率を与えることを明らかにした。
n−ブチルアミンの不在下で実施例1の操作を繰り返し、使用されたDFFを基準として7%の収率に相当する、たったの18mgのFDAが得られた。
0.4ミリモルのn−ブチルアミンをRaney CoとDFFとの混合物中へ導入したことを除いて、実施例1の操作を繰り返した。使用されたDFFを基準として25%の収率に相当する、63mgのFDAが得られた。
2.0ミリモルのn−ブチルアミンをRaney CoとDFFとの混合物中へ導入したことを除いて、実施例1の操作を繰り返した。使用されたDFFを基準として38%の収率に相当する、96mgのFDAが得られた。
120mgのPricat Ni 52/35、2.0ミリモルのDFFおよび6.0ミリモルのn−ブチルアミンを含有する100mLのParr反応器に25mLのメタノールを導入した。反応器を次に3回窒素でパージし、混合物を0.2MPaアンモニアの雰囲気下でかき混ぜてアルコール中におおよそ2gのアンモニアを溶解させた。水素を次に反応器へ導入して2MPaの水素分圧を提供し、反応は次に115〜120℃の温度で4時間進行した。反応の完了後に、反応器を冷まし、未反応アンモニアを放出した。ガスクロマトグラフィーによる反応器中の残留液相の分析は、55mgのFDAおよび44mgのテトラヒドロフラン−2,5−ジメチルアミン(THFDA)が得られ、使用されたDFFを基準とする収率がそれぞれ、22%および17%であることを明らかにした。
120mgのNi/PrO2−CeO2触媒、2.0ミリモルのDFFおよび6.0ミリモルのn−ブチルアミンを含有する100mLのParr反応器に、25mLのメタノールを導入した。反応器を次に3回窒素でパージし、混合物を0.2MPaアンモニアの雰囲気下でかき混ぜてアルコール中におおよそ2gのアンモニアを溶解させた。水素を次に反応器へ導入して2MPaの水素分圧を提供し、反応は次に115〜120℃の温度で4時間進行した。反応の完了後に、反応器を冷まし、未反応アンモニアを放出した。ガスクロマトグラフィーによる反応器中の残留液相の分析は、114mgのFDAが得られ、DFFを基準として45%の収率を与えることを明らかにした。
120mgのCuNiOx触媒、2.0ミリモルのDFFおよび6.0ミリモルのn−ブチルアミンを含有する100mLのParr反応器に、25mLのメタノールを導入した。反応器を次に3回窒素でパージし、混合物を0.2MPaアンモニアの雰囲気下でかき混ぜてアルコール中におおよそ2gのアンモニアを溶解させた。水素を次に反応器へ導入して2MPaの水素分圧を提供し、反応は次に115〜120℃の温度で4時間進行した。反応の完了後に、反応器を冷まし、未反応アンモニアを放出した。ガスクロマトグラフィーによる反応器中の残留液相の分析は、124mgのFDAが得られ、DFFを基準として49%の収率を与えることを明らかにした。
120mgのCuNiOx触媒、2.0ミリモルのDFFおよび6.0ミリモルのn−ブチルアミンを含有する100mLのParr反応器に、25mLのメタノールを導入した。反応器を次に3回窒素でパージし、混合物を0.2MPaアンモニアの雰囲気下でかき混ぜてアルコール中におおよそ2gのアンモニアを溶解させた。水素を次に反応器へ導入して2MPaの水素分圧を提供し、反応は次に80℃の温度で15時間進行した。反応の完了後に、反応器を冷まし、未反応アンモニアを放出した。ガスクロマトグラフィーによる反応器中の残留液相の分析は、211mgのFDAが得られ、DFFを基準として84%の収率を与えることを明らかにした。
Claims (17)
- 芳香族第一級アミンの製造方法であって、前記方法が、水素化触媒およびアミンの存在下で、芳香族ジアルデヒドを水素およびアンモニアと反応させる工程を含み、
アミンが、
メチルアミン、エチルアミン、プロピルアミン、ブチルアミン、ペンチルアミン、ヘキシルアミン、ベンジルアミン、シクロヘキシルアミン、およびエチレンジアミンからなる群から選択される第一級アミンであり、
芳香族ジアルデヒドに対するアミンのモル比が反応の開始時に0.25以上であり、芳香族ジアルデヒドが2,5−ジホルミルフランである、方法。 - 第一級アミンが、メチルアミン、ブチルアミン、ペンチルアミンおよびヘキシルアミンからなる群から選択される、請求項1に記載の方法。
- 第一級アミンが、メチルアミンおよびブチルアミンからなる群から選択される、請求項1または2に記載の方法
- 芳香族ジアルデヒドに対するアミンのモル比が、反応の開始時に、0.25以上である、請求項1〜3のいずれか一項に記載の方法。
- 芳香族ジアルデヒドに対するアミンのモル比が、反応の開始時に、0.5以上である、請求項1〜4のいずれか一項に記載の方法。
- 芳香族ジアルデヒドに対するアミンのモル比が、反応の開始時に、1以上である、請求項1〜5のいずれか一項に記載の方法。
- 芳香族ジアルデヒドに対するアミンのモル比が、反応の開始時に、4以下である、請求項1〜6のいずれか一項に記載の方法。
- 芳香族ジアルデヒドに対するアミンのモル比が、反応の開始時に、3以下である、請求項1〜7のいずれか一項に記載の方法。
- 芳香族ジアルデヒドに対するアミンのモル比が、反応の開始時に、2以下である、請求項1〜8のいずれか一項に記載の方法。
- 芳香族ジアルデヒド対アンモニアのモル比が、1:2〜1:50の範囲にあり、アンモニアが、導入されたアンモニアである、請求項1〜9のいずれか一項に記載の方法。
- 芳香族ジアルデヒド対アンモニアのモル比が、1:5〜1:20の範囲にあり、アンモニアが、導入されたアンモニアである、請求項1〜10のいずれか一項に記載の方法。
- 芳香族ジアルデヒドが、芳香族ジアルデヒドに対するアミンのモル比が反応の全体にわたって0.25以上であることを確実にするためのやり方で供給される、請求項1〜11のいずれか一項に記載の方法。
- 芳香族ジアルデヒドが、芳香族ジアルデヒドに対するアミンのモル比が反応の全体にわたって0.25〜2の範囲にあることを確実にするためのやり方で供給される、請求項1〜12のいずれか一項に記載の方法。
- 芳香族ジアルデヒドが、芳香族ジアルデヒドに対するアミンのモル比が反応の全体にわたって1〜2の範囲にあることを確実にするためのやり方で供給される、請求項1〜13のいずれか一項に記載の方法。
- 反応温度が、40〜200℃の範囲にある、請求項1〜14のいずれか一項に記載の方法。
- 反応温度が、100〜150℃の範囲にある、請求項1〜15のいずれか一項に記載の方法。
- 芳香族ジアミンが2,5−ビス(アミノメチル)フランである、請求項1〜16のいずれか一項に記載の方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2014081945 | 2014-07-10 | ||
CNPCT/CN2014/081945 | 2014-07-10 | ||
PCT/CN2015/083535 WO2016004867A1 (en) | 2014-07-10 | 2015-07-08 | Process for producing aromatic primary diamines |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2017521430A JP2017521430A (ja) | 2017-08-03 |
JP2017521430A5 JP2017521430A5 (ja) | 2019-06-27 |
JP6704896B2 true JP6704896B2 (ja) | 2020-06-03 |
Family
ID=55063589
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2017500926A Active JP6704896B2 (ja) | 2014-07-10 | 2015-07-08 | 芳香族第一級ジアミンの製造方法 |
Country Status (7)
Country | Link |
---|---|
US (2) | US10899726B2 (ja) |
EP (2) | EP3674285B1 (ja) |
JP (1) | JP6704896B2 (ja) |
KR (1) | KR20170027792A (ja) |
CN (2) | CN111116528B (ja) |
BR (1) | BR112017000203B1 (ja) |
WO (1) | WO2016004867A1 (ja) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6714072B2 (ja) * | 2016-03-29 | 2020-06-24 | 株式会社日本触媒 | 複素環を有するジアミン化合物の製造方法 |
WO2018085957A1 (en) * | 2016-11-09 | 2018-05-17 | Rhodia Operations | Process for production of aromatic compounds comprising at least two amine functions |
EP3656766B1 (en) * | 2017-07-21 | 2021-09-15 | Mitsubishi Gas Chemical Company, Inc. | Method for producing 2,5-bis(aminomethyl)furan |
EP3696172B1 (en) * | 2017-10-11 | 2023-05-31 | Mitsubishi Gas Chemical Company, Inc. | Method for producing 2,5-bis (aminomethyl) tetrahydrofuran |
EP3696173B1 (en) * | 2017-10-11 | 2021-12-22 | Mitsubishi Gas Chemical Company, Inc. | Method for producing 2,5-bis(aminomethyl) tetrahydrofuran |
CN111097421A (zh) * | 2018-10-29 | 2020-05-05 | 中国科学院大连化学物理研究所 | 负载型金属催化剂及其催化醛类化合物制备伯胺的方法 |
CN114602461B (zh) * | 2020-12-09 | 2023-04-07 | 中国科学院大连化学物理研究所 | 一种催化二元醛制备二元胺的方法 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2636051A (en) | 1948-04-05 | 1953-04-21 | Shell Dev | Preparation of diamine |
DE2824423A1 (de) | 1978-06-03 | 1979-12-06 | Ruhrchemie Ag | Verfahren zur herstellung von diaminen |
JPS60146885A (ja) | 1984-01-06 | 1985-08-02 | Mitsubishi Petrochem Co Ltd | フルフリルアミン及び/又はテトラヒドロフルフリルアミンの製造法 |
JPS62446A (ja) | 1985-06-25 | 1987-01-06 | Mitsubishi Petrochem Co Ltd | 脂肪芳香族アミンの製造方法 |
DE3822038A1 (de) | 1988-06-30 | 1990-03-01 | Hoechst Ag | Verfahren zur herstellung von 3(4),8(9)-bis-(aminomethyl)-tricyclo (5.2.1.0(pfeil hoch)2(pfeil hoch)(pfeil hoch),(pfeil hoch)(pfeil hoch)6(pfeil hoch))-decan |
DE3917444A1 (de) | 1989-05-30 | 1991-02-21 | Hoechst Ag | Verfahren zur herstellung von (alpha),(omega)-diaminen |
JP3001685B2 (ja) | 1991-07-09 | 2000-01-24 | 広栄化学工業株式会社 | ジアミンの製造法 |
AT399149B (de) | 1993-06-07 | 1995-03-27 | Chemie Linz Gmbh | Verfahren zur herstellung primärer amine aus aldehyden |
JP3630709B2 (ja) | 1993-12-28 | 2005-03-23 | 株式会社クラレ | 脂肪族ジアミンの製造方法 |
JPH10130210A (ja) * | 1996-10-29 | 1998-05-19 | Kuraray Co Ltd | ジアミンの製造方法 |
JPH10310559A (ja) | 1997-05-09 | 1998-11-24 | Kuraray Co Ltd | ジアミンの製造方法 |
CA2419519A1 (en) | 2002-03-27 | 2003-09-27 | Kuraray Co., Ltd. | Process for producing diamines |
DE102004023529A1 (de) * | 2004-05-13 | 2005-12-08 | Basf Ag | Verfahren zur kontinuierlichen Herstellung eines Amins |
ZA200800825B (en) * | 2005-06-30 | 2009-04-29 | Dow Global Technologies Inc | Process for the reductive amination of aldehydes and ketons via the formation of macrocyclic polyimine intermediates |
CN101600681B (zh) * | 2006-12-15 | 2013-09-18 | 陶氏环球技术有限责任公司 | 醛和酮的还原胺化方法 |
DE102010030991A1 (de) * | 2010-07-06 | 2012-01-12 | Evonik Degussa Gmbh | Verfahren zur Herstellung von 2,5-Diformylfuran und seiner Derivate |
-
2015
- 2015-07-08 CN CN201911137833.1A patent/CN111116528B/zh active Active
- 2015-07-08 WO PCT/CN2015/083535 patent/WO2016004867A1/en active Application Filing
- 2015-07-08 KR KR1020177002283A patent/KR20170027792A/ko not_active Application Discontinuation
- 2015-07-08 BR BR112017000203-5A patent/BR112017000203B1/pt active IP Right Grant
- 2015-07-08 EP EP20157956.2A patent/EP3674285B1/en active Active
- 2015-07-08 EP EP15819072.8A patent/EP3166921B1/en active Active
- 2015-07-08 JP JP2017500926A patent/JP6704896B2/ja active Active
- 2015-07-08 US US15/324,932 patent/US10899726B2/en active Active
- 2015-07-08 CN CN201580037775.9A patent/CN106488905B/zh active Active
-
2020
- 2020-02-04 US US16/781,356 patent/US11066377B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
CN111116528A (zh) | 2020-05-08 |
US10899726B2 (en) | 2021-01-26 |
EP3166921B1 (en) | 2020-02-19 |
BR112017000203B1 (pt) | 2020-12-08 |
EP3166921A1 (en) | 2017-05-17 |
US20170217916A1 (en) | 2017-08-03 |
WO2016004867A1 (en) | 2016-01-14 |
EP3674285B1 (en) | 2022-04-06 |
CN106488905A (zh) | 2017-03-08 |
EP3674285A1 (en) | 2020-07-01 |
KR20170027792A (ko) | 2017-03-10 |
EP3166921A4 (en) | 2018-01-24 |
US11066377B2 (en) | 2021-07-20 |
JP2017521430A (ja) | 2017-08-03 |
BR112017000203A2 (pt) | 2018-01-16 |
CN106488905B (zh) | 2019-12-17 |
CN111116528B (zh) | 2023-08-01 |
US20200172501A1 (en) | 2020-06-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6704896B2 (ja) | 芳香族第一級ジアミンの製造方法 | |
JP5846126B2 (ja) | 芳香族アルコール又は複素環式芳香族アルコールの製造方法 | |
JP2019529395A (ja) | ZrO2上に担持されたルテニウム触媒の存在下でのニトリル水素化のための方法 | |
JP2004516308A (ja) | ニトリルおよびイミンの水素化により第一級および第二級アミンを製造する方法 | |
JPH0368541A (ja) | カルボニルのアミノ化 | |
TWI720968B (zh) | 雙(胺甲基)環己烷之異構化方法 | |
JP2008143832A (ja) | 脂環式アミン又は飽和複素環式アミンの製造方法 | |
ES2542065T3 (es) | Método de fabricación de metilpentametilen diamina y metilpiperidina | |
Hammerschmidt et al. | Copper catalyzed synthesis of cyclic amines from amino-alcohols | |
TWI482749B (zh) | 由二氟乙腈製備2,2-二氟乙胺及其鹽類之方法 | |
US7119230B2 (en) | Process for production of xylylenediamine and/or cyanobenzylamine | |
JP2011225502A5 (ja) | ||
JP4692700B2 (ja) | 芳香族シアノアミノメチルの製造方法 | |
JP5739590B1 (ja) | メタ−キシリレンジイソシアネート類の製造方法 | |
TWI785127B (zh) | 2,5-雙(胺甲基)四氫呋喃之製造方法 | |
JP4561963B2 (ja) | ジ(アミノメチル)置換芳香族化合物の高選択的な製造方法 | |
EP2699538B1 (en) | Process for the preparation of alkyldiamines | |
Lan et al. | Metal catalyst-free amination of 2-chloro-5-nitrobenzoic acid in superheated water | |
JP5658508B2 (ja) | 第三級アミンの製造方法 | |
JP2023117830A (ja) | ビテトラヒドロフランジカルボン酸化合物及びその製造方法 | |
Cordier | Influence of the Medium on Hydrogenation of 2-Methylglutaronitrile Selective Access to β-Methylpentane Diamine or p-Picoline after Dehydrogenation | |
BRPI0906230B1 (pt) | Methyl-2-pentamethylene diamine and methyl-3-piperidine manufacturing process | |
CN103159635A (zh) | 一种制备4-甲氧基-n-4-甲苯基苯胺的方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20180608 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20190207 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20190226 |
|
A524 | Written submission of copy of amendment under article 19 pct |
Free format text: JAPANESE INTERMEDIATE CODE: A524 Effective date: 20190524 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20191029 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20200221 |
|
A911 | Transfer to examiner for re-examination before appeal (zenchi) |
Free format text: JAPANESE INTERMEDIATE CODE: A911 Effective date: 20200303 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20200414 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20200513 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 6704896 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |