JP5451746B2 - ニトロ化炭化水素、誘導体及びそれらの製造プロセス - Google Patents
ニトロ化炭化水素、誘導体及びそれらの製造プロセス Download PDFInfo
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- JP5451746B2 JP5451746B2 JP2011505090A JP2011505090A JP5451746B2 JP 5451746 B2 JP5451746 B2 JP 5451746B2 JP 2011505090 A JP2011505090 A JP 2011505090A JP 2011505090 A JP2011505090 A JP 2011505090A JP 5451746 B2 JP5451746 B2 JP 5451746B2
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- Prior art keywords
- alkyl
- cycloalkyl
- nitro
- amino
- formula
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- 238000000034 method Methods 0.000 title claims description 86
- 230000008569 process Effects 0.000 title claims description 67
- 150000002430 hydrocarbons Chemical class 0.000 title claims description 61
- 229930195733 hydrocarbon Natural products 0.000 title claims description 60
- 238000004519 manufacturing process Methods 0.000 title claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 168
- 229910052799 carbon Inorganic materials 0.000 claims description 90
- 150000001875 compounds Chemical class 0.000 claims description 77
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 72
- 229910052739 hydrogen Inorganic materials 0.000 claims description 56
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 55
- 125000003118 aryl group Chemical group 0.000 claims description 46
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 40
- 229910017604 nitric acid Inorganic materials 0.000 claims description 38
- 239000004215 Carbon black (E152) Substances 0.000 claims description 32
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 29
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 24
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 24
- 239000003054 catalyst Substances 0.000 claims description 23
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 21
- 150000001414 amino alcohols Chemical class 0.000 claims description 19
- 238000006396 nitration reaction Methods 0.000 claims description 18
- 238000005984 hydrogenation reaction Methods 0.000 claims description 12
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 11
- WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 8
- 125000000160 oxazolidinyl group Chemical group 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 150000001335 aliphatic alkanes Chemical group 0.000 claims description 4
- 238000009833 condensation Methods 0.000 claims description 4
- 230000005494 condensation Effects 0.000 claims description 4
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 3
- 230000002152 alkylating effect Effects 0.000 claims description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 description 43
- 239000000243 solution Substances 0.000 description 22
- 239000000047 product Substances 0.000 description 21
- 239000003795 chemical substances by application Substances 0.000 description 19
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 239000000203 mixture Substances 0.000 description 18
- -1 nitroalkanes Chemical class 0.000 description 15
- 239000000376 reactant Substances 0.000 description 14
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 230000003647 oxidation Effects 0.000 description 11
- 238000007254 oxidation reaction Methods 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- 239000003921 oil Substances 0.000 description 10
- SUGZATOHBPXTDV-UHFFFAOYSA-N 2-nitrobutane Chemical compound CCC(C)[N+]([O-])=O SUGZATOHBPXTDV-UHFFFAOYSA-N 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 9
- 125000001424 substituent group Chemical group 0.000 description 9
- 150000001299 aldehydes Chemical class 0.000 description 8
- 239000007791 liquid phase Substances 0.000 description 8
- 238000012856 packing Methods 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 7
- 229920003986 novolac Polymers 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 239000006227 byproduct Substances 0.000 description 6
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 5
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 5
- 125000004429 atom Chemical group 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 239000002516 radical scavenger Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 4
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 4
- 229910000564 Raney nickel Inorganic materials 0.000 description 4
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 150000001924 cycloalkanes Chemical class 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 239000004814 polyurethane Substances 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- ASNUCXNSIMBBMA-UHFFFAOYSA-N 2-amino-2-ethylheptan-1-ol Chemical compound CCCCCC(N)(CC)CO ASNUCXNSIMBBMA-UHFFFAOYSA-N 0.000 description 3
- KIOCABJEBRVQNM-UHFFFAOYSA-N 2-amino-2-methylhexan-1-ol Chemical compound CCCCC(C)(N)CO KIOCABJEBRVQNM-UHFFFAOYSA-N 0.000 description 3
- PUHONNHQBPIIJT-UHFFFAOYSA-N 2-amino-2-propylhexan-1-ol Chemical compound CCCCC(N)(CO)CCC PUHONNHQBPIIJT-UHFFFAOYSA-N 0.000 description 3
- HNHLSWMRWNEGNV-UHFFFAOYSA-N 2-ethyl-2-nitroheptan-1-ol Chemical compound CCCCCC(CC)(CO)[N+]([O-])=O HNHLSWMRWNEGNV-UHFFFAOYSA-N 0.000 description 3
- DIHHDRFCNKCLRC-UHFFFAOYSA-N 2-ethyl-2-nitropentan-1-ol Chemical compound CCCC(CC)(CO)[N+]([O-])=O DIHHDRFCNKCLRC-UHFFFAOYSA-N 0.000 description 3
- NDQJYXKPCFULDQ-UHFFFAOYSA-N 2-hexyl-2-nitrononan-1-ol Chemical compound CCCCCCCC(CO)([N+]([O-])=O)CCCCCC NDQJYXKPCFULDQ-UHFFFAOYSA-N 0.000 description 3
- DRIGEMGHEMSMAJ-UHFFFAOYSA-N 2-methyl-2-nitrohexan-1-ol Chemical compound CCCCC(C)(CO)[N+]([O-])=O DRIGEMGHEMSMAJ-UHFFFAOYSA-N 0.000 description 3
- SUWXVLPNJUWCKI-UHFFFAOYSA-N 2-methyl-2-nitrooctan-1-ol Chemical compound CCCCCCC(C)(CO)[N+]([O-])=O SUWXVLPNJUWCKI-UHFFFAOYSA-N 0.000 description 3
- WXOHMWXKXPWTBA-UHFFFAOYSA-N 2-nitro-2-propylhexan-1-ol Chemical compound CCCCC(CO)([N+]([O-])=O)CCC WXOHMWXKXPWTBA-UHFFFAOYSA-N 0.000 description 3
- AYHGEUIBJJHENQ-UHFFFAOYSA-N 4-methyl-4-propyl-1,3-oxazolidine Chemical compound CCCC1(C)COCN1 AYHGEUIBJJHENQ-UHFFFAOYSA-N 0.000 description 3
- ITIMFQOKJZOHRG-UHFFFAOYSA-N 4-undecyl-1,3-oxazolidine Chemical compound CCCCCCCCCCCC1COCN1 ITIMFQOKJZOHRG-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 3
- 239000007868 Raney catalyst Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000003115 biocidal effect Effects 0.000 description 3
- 239000003139 biocide Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000004817 gas chromatography Methods 0.000 description 3
- 239000013529 heat transfer fluid Substances 0.000 description 3
- 239000001282 iso-butane Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 239000003345 natural gas Substances 0.000 description 3
- 230000003472 neutralizing effect Effects 0.000 description 3
- LFLZOWIFJOBEPN-UHFFFAOYSA-N nitrate, nitrate Chemical compound O[N+]([O-])=O.O[N+]([O-])=O LFLZOWIFJOBEPN-UHFFFAOYSA-N 0.000 description 3
- 230000000802 nitrating effect Effects 0.000 description 3
- 125000004971 nitroalkyl group Chemical group 0.000 description 3
- 150000002917 oxazolidines Chemical class 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- FTOCRXXRFVICFT-UHFFFAOYSA-N (1-aminocyclodecyl)methanol Chemical compound OCC1(N)CCCCCCCCC1 FTOCRXXRFVICFT-UHFFFAOYSA-N 0.000 description 2
- VDPLLINNMXFNQX-UHFFFAOYSA-N (1-aminocyclohexyl)methanol Chemical compound OCC1(N)CCCCC1 VDPLLINNMXFNQX-UHFFFAOYSA-N 0.000 description 2
- RNMJPIYVCVKBMG-UHFFFAOYSA-N (1-aminocyclononyl)methanol Chemical compound OCC1(N)CCCCCCCC1 RNMJPIYVCVKBMG-UHFFFAOYSA-N 0.000 description 2
- SWZDYPQVZUVWPA-UHFFFAOYSA-N (1-aminocycloundecyl)methanol Chemical compound OCC1(N)CCCCCCCCCC1 SWZDYPQVZUVWPA-UHFFFAOYSA-N 0.000 description 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 description 2
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
- GOLOHAZKJYGKKQ-UHFFFAOYSA-N 1-nitrodecane Chemical compound CCCCCCCCCC[N+]([O-])=O GOLOHAZKJYGKKQ-UHFFFAOYSA-N 0.000 description 2
- MQEMKUTWMALMCC-UHFFFAOYSA-N 1-nitrododecane Chemical compound CCCCCCCCCCCC[N+]([O-])=O MQEMKUTWMALMCC-UHFFFAOYSA-N 0.000 description 2
- OGBHSDXSHOMXHS-UHFFFAOYSA-N 1-nitroheptadecane Chemical compound CCCCCCCCCCCCCCCCC[N+]([O-])=O OGBHSDXSHOMXHS-UHFFFAOYSA-N 0.000 description 2
- LMTCHMNYSSJHPG-UHFFFAOYSA-N 1-nitrohexadecane Chemical compound CCCCCCCCCCCCCCCC[N+]([O-])=O LMTCHMNYSSJHPG-UHFFFAOYSA-N 0.000 description 2
- KLGHUFNKRIWCDQ-UHFFFAOYSA-N 1-nitrooctane Chemical compound CCCCCCCC[N+]([O-])=O KLGHUFNKRIWCDQ-UHFFFAOYSA-N 0.000 description 2
- GQUKFPOTLYZVDB-UHFFFAOYSA-N 1-nitropentadecane Chemical compound CCCCCCCCCCCCCCC[N+]([O-])=O GQUKFPOTLYZVDB-UHFFFAOYSA-N 0.000 description 2
- SWSHTNVBBCEYKR-UHFFFAOYSA-N 1-nitrotetradecane Chemical compound CCCCCCCCCCCCCC[N+]([O-])=O SWSHTNVBBCEYKR-UHFFFAOYSA-N 0.000 description 2
- OVJFXQPAVMVKOV-UHFFFAOYSA-N 1-nitrotridecane Chemical compound CCCCCCCCCCCCC[N+]([O-])=O OVJFXQPAVMVKOV-UHFFFAOYSA-N 0.000 description 2
- KWIRDGZOAKOCGD-UHFFFAOYSA-N 1-nitroundecane Chemical compound CCCCCCCCCCC[N+]([O-])=O KWIRDGZOAKOCGD-UHFFFAOYSA-N 0.000 description 2
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical compound CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 2
- PPARDJLBOXOBKV-UHFFFAOYSA-N 2-amino-2-butyldecan-1-ol Chemical compound CCCCCCCCC(N)(CO)CCCC PPARDJLBOXOBKV-UHFFFAOYSA-N 0.000 description 2
- RBRIIYTYFVXMHT-UHFFFAOYSA-N 2-amino-2-butyldodecan-1-ol Chemical compound CCCCCCCCCCC(N)(CO)CCCC RBRIIYTYFVXMHT-UHFFFAOYSA-N 0.000 description 2
- GSXBEQWNPZIBLZ-UHFFFAOYSA-N 2-amino-2-butylheptan-1-ol Chemical compound CCCCCC(N)(CO)CCCC GSXBEQWNPZIBLZ-UHFFFAOYSA-N 0.000 description 2
- RDEFHGRTIKHVTK-UHFFFAOYSA-N 2-amino-2-butylhexan-1-ol Chemical compound CCCCC(N)(CO)CCCC RDEFHGRTIKHVTK-UHFFFAOYSA-N 0.000 description 2
- PZAFLOVABHSEPL-UHFFFAOYSA-N 2-amino-2-butylnonan-1-ol Chemical compound CCCCCCCC(N)(CO)CCCC PZAFLOVABHSEPL-UHFFFAOYSA-N 0.000 description 2
- SXUDFXVTAJOHJR-UHFFFAOYSA-N 2-amino-2-butyloctan-1-ol Chemical compound CCCCCCC(N)(CO)CCCC SXUDFXVTAJOHJR-UHFFFAOYSA-N 0.000 description 2
- ALEQUIXUQJYJNI-UHFFFAOYSA-N 2-amino-2-butyltetradecan-1-ol Chemical compound CCCCCCCCCCCCC(N)(CO)CCCC ALEQUIXUQJYJNI-UHFFFAOYSA-N 0.000 description 2
- XVYUYFQZPKRZJL-UHFFFAOYSA-N 2-amino-2-butyltridecan-1-ol Chemical compound CCCCCCCCCCCC(N)(CO)CCCC XVYUYFQZPKRZJL-UHFFFAOYSA-N 0.000 description 2
- JNDXUAXLQOAMFW-UHFFFAOYSA-N 2-amino-2-butylundecan-1-ol Chemical compound CCCCCCCCCC(N)(CO)CCCC JNDXUAXLQOAMFW-UHFFFAOYSA-N 0.000 description 2
- SISCNWJENSMCII-UHFFFAOYSA-N 2-amino-2-decylpropane-1,3-diol Chemical compound CCCCCCCCCCC(N)(CO)CO SISCNWJENSMCII-UHFFFAOYSA-N 0.000 description 2
- PAJZSLNFQZKPAG-UHFFFAOYSA-N 2-amino-2-dodecylpropane-1,3-diol Chemical compound CCCCCCCCCCCCC(N)(CO)CO PAJZSLNFQZKPAG-UHFFFAOYSA-N 0.000 description 2
- CFRALWJZNSPUIW-UHFFFAOYSA-N 2-amino-2-ethyldodecan-1-ol Chemical compound CCCCCCCCCCC(N)(CC)CO CFRALWJZNSPUIW-UHFFFAOYSA-N 0.000 description 2
- QLCLMKXZLUDTKF-UHFFFAOYSA-N 2-amino-2-ethylheptadecan-1-ol Chemical compound CCCCCCCCCCCCCCCC(N)(CC)CO QLCLMKXZLUDTKF-UHFFFAOYSA-N 0.000 description 2
- GTWCTYQCWJAURK-UHFFFAOYSA-N 2-amino-2-ethylhexadecan-1-ol Chemical compound CCCCCCCCCCCCCCC(N)(CC)CO GTWCTYQCWJAURK-UHFFFAOYSA-N 0.000 description 2
- AQVAKYWHEGYKEE-UHFFFAOYSA-N 2-amino-2-ethylhexan-1-ol Chemical compound CCCCC(N)(CC)CO AQVAKYWHEGYKEE-UHFFFAOYSA-N 0.000 description 2
- YRJHDFPUSLCJBF-UHFFFAOYSA-N 2-amino-2-ethyloctan-1-ol Chemical compound CCCCCCC(N)(CC)CO YRJHDFPUSLCJBF-UHFFFAOYSA-N 0.000 description 2
- PDVDVCSVYXZLOI-UHFFFAOYSA-N 2-amino-2-ethylpentan-1-ol Chemical compound CCCC(N)(CC)CO PDVDVCSVYXZLOI-UHFFFAOYSA-N 0.000 description 2
- SXONRXQDGMPOBM-UHFFFAOYSA-N 2-amino-2-ethyltetradecan-1-ol Chemical compound CCCCCCCCCCCCC(N)(CC)CO SXONRXQDGMPOBM-UHFFFAOYSA-N 0.000 description 2
- COXBBBFLQROKPD-UHFFFAOYSA-N 2-amino-2-ethylundecan-1-ol Chemical compound CCCCCCCCCC(N)(CC)CO COXBBBFLQROKPD-UHFFFAOYSA-N 0.000 description 2
- ZWHNDGIMMDARIZ-UHFFFAOYSA-N 2-amino-2-heptadecylpropane-1,3-diol Chemical compound CCCCCCCCCCCCCCCCCC(N)(CO)CO ZWHNDGIMMDARIZ-UHFFFAOYSA-N 0.000 description 2
- TWARLPUHZFJERI-UHFFFAOYSA-N 2-amino-2-heptyldecan-1-ol Chemical compound CCCCCCCCC(N)(CO)CCCCCCC TWARLPUHZFJERI-UHFFFAOYSA-N 0.000 description 2
- KVEDZMPCSNBSED-UHFFFAOYSA-N 2-amino-2-heptyldodecan-1-ol Chemical compound CCCCCCCCCCC(N)(CO)CCCCCCC KVEDZMPCSNBSED-UHFFFAOYSA-N 0.000 description 2
- NBXJGTRNWIMNDY-UHFFFAOYSA-N 2-amino-2-heptylnonan-1-ol Chemical compound CCCCCCCC(N)(CO)CCCCCCC NBXJGTRNWIMNDY-UHFFFAOYSA-N 0.000 description 2
- RICHFGXGSKPCFA-UHFFFAOYSA-N 2-amino-2-heptylpropane-1,3-diol Chemical compound CCCCCCCC(N)(CO)CO RICHFGXGSKPCFA-UHFFFAOYSA-N 0.000 description 2
- GQOOSXHYVDMHSW-UHFFFAOYSA-N 2-amino-2-heptylundecan-1-ol Chemical compound CCCCCCCCCC(N)(CO)CCCCCCC GQOOSXHYVDMHSW-UHFFFAOYSA-N 0.000 description 2
- NUDVTLPOESYOSC-UHFFFAOYSA-N 2-amino-2-hexadecylpropane-1,3-diol Chemical compound CCCCCCCCCCCCCCCCC(N)(CO)CO NUDVTLPOESYOSC-UHFFFAOYSA-N 0.000 description 2
- KDNBAOXYAKVCJP-UHFFFAOYSA-N 2-amino-2-hexyldecan-1-ol Chemical compound CCCCCCCCC(N)(CO)CCCCCC KDNBAOXYAKVCJP-UHFFFAOYSA-N 0.000 description 2
- XDFFTUMGOCPICA-UHFFFAOYSA-N 2-amino-2-hexyldodecan-1-ol Chemical compound CCCCCCCCCCC(N)(CO)CCCCCC XDFFTUMGOCPICA-UHFFFAOYSA-N 0.000 description 2
- DZWCHNPQIMRUAA-UHFFFAOYSA-N 2-amino-2-hexylnonan-1-ol Chemical compound CCCCCCCC(N)(CO)CCCCCC DZWCHNPQIMRUAA-UHFFFAOYSA-N 0.000 description 2
- REYKUHUGOJZQGV-UHFFFAOYSA-N 2-amino-2-hexyloctan-1-ol Chemical compound CCCCCCC(N)(CO)CCCCCC REYKUHUGOJZQGV-UHFFFAOYSA-N 0.000 description 2
- OVPDRXFLFKTUQM-UHFFFAOYSA-N 2-amino-2-hexyltridecan-1-ol Chemical compound CCCCCCCCCCCC(N)(CO)CCCCCC OVPDRXFLFKTUQM-UHFFFAOYSA-N 0.000 description 2
- NDSNTIXWPUOZBW-UHFFFAOYSA-N 2-amino-2-methyldodecan-1-ol Chemical compound CCCCCCCCCCC(C)(N)CO NDSNTIXWPUOZBW-UHFFFAOYSA-N 0.000 description 2
- WKPYYYNLWREQNC-UHFFFAOYSA-N 2-amino-2-methylheptadecan-1-ol Chemical compound CCCCCCCCCCCCCCCC(C)(N)CO WKPYYYNLWREQNC-UHFFFAOYSA-N 0.000 description 2
- BUSOXNRPZDZCKM-UHFFFAOYSA-N 2-amino-2-methylheptan-1-ol Chemical compound CCCCCC(C)(N)CO BUSOXNRPZDZCKM-UHFFFAOYSA-N 0.000 description 2
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- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000005932 reductive alkylation reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
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- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 1
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- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
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Classifications
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- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
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- A—HUMAN NECESSITIES
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
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- A—HUMAN NECESSITIES
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
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- C—CHEMISTRY; METALLURGY
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
- C07C201/06—Preparation of nitro compounds
- C07C201/08—Preparation of nitro compounds by substitution of hydrogen atoms by nitro groups
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
- C07C201/06—Preparation of nitro compounds
- C07C201/12—Preparation of nitro compounds by reactions not involving the formation of nitro groups
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/01—Compounds containing nitro groups bound to a carbon skeleton having nitro groups bound to acyclic carbon atoms
- C07C205/02—Compounds containing nitro groups bound to a carbon skeleton having nitro groups bound to acyclic carbon atoms of a saturated carbon skeleton
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- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/01—Compounds containing nitro groups bound to a carbon skeleton having nitro groups bound to acyclic carbon atoms
- C07C205/03—Compounds containing nitro groups bound to a carbon skeleton having nitro groups bound to acyclic carbon atoms of an unsaturated carbon skeleton
- C07C205/04—Compounds containing nitro groups bound to a carbon skeleton having nitro groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing six-membered aromatic rings
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/06—Compounds containing nitro groups bound to a carbon skeleton having nitro groups bound to carbon atoms of six-membered aromatic rings
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/13—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups
- C07C205/14—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups and hydroxy groups bound to acyclic carbon atoms
- C07C205/15—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups and hydroxy groups bound to acyclic carbon atoms of a saturated carbon skeleton
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- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/13—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups
- C07C205/14—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups and hydroxy groups bound to acyclic carbon atoms
- C07C205/16—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups and hydroxy groups bound to acyclic carbon atoms of a carbon skeleton containing six-membered aromatic rings
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- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
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- C07C205/18—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups or hydroxy groups bound to carbon atoms of rings other than six-membered aromatic rings
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/02—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions involving the formation of amino groups from compounds containing hydroxy groups or etherified or esterified hydroxy groups
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- C07C215/04—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
- C07C215/06—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic
- C07C215/08—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic with only one hydroxy group and one amino group bound to the carbon skeleton
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- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/04—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
- C07C215/06—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic
- C07C215/10—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic with one amino group and at least two hydroxy groups bound to the carbon skeleton
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- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/04—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
- C07C215/20—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated the carbon skeleton being saturated and containing rings
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- C—CHEMISTRY; METALLURGY
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/22—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated
- C07C215/28—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings
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- C07C215/42—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having amino groups or hydroxy groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
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- C—CHEMISTRY; METALLURGY
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C239/00—Compounds containing nitrogen-to-halogen bonds; Hydroxylamino compounds or ethers or esters thereof
- C07C239/08—Hydroxylamino compounds or their ethers or esters
- C07C239/10—Hydroxylamino compounds or their ethers or esters having nitrogen atoms of hydroxylamino groups further bound to carbon atoms of unsubstituted hydrocarbon radicals or of hydrocarbon radicals substituted by halogen atoms or by nitro or nitroso groups
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- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/04—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
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- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
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- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3271—Hydroxyamines
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- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
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- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
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- C07C2602/00—Systems containing two condensed rings
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- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
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- 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
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Description
本件特許出願は2008年4月16日出願の米国仮特許出願第61/045,380号の利益を請求する。
本発明は、ニトロ化炭化水素、例えばニトロアルカン、ニトロシクロアルカン及びニトロアラルキルの製造プロセス並びにニトロ化炭化水素の誘導化合物の製造プロセスに関する。本発明は新規なニトロ化炭化水素及び新規な誘導体にも関する。
の化合物が含まれる。RがC2〜C8アルキル又はC3〜C8シクロアルキルである式(I)の化合物が更に好ましい。R1及びRyの一方がアルキル基である化合物も好ましい。
のニトロアルコールの製造のためのプロセスが提供される。この態様のプロセスは、(a)前記のようにして製造された、式(I)(式中、RyはHである)のニトロ化炭化水素を用意し、そして(b)このニトロ化炭化水素をアルデヒドと、アルカリ性触媒の存在下で縮合させることを含んでなる。
のアミノアルコールの製造のためのプロセスが提供される。この態様のプロセスは、(a)前記のようにして製造された、式(II)のニトロアルコールを用意し、そして(b)このニトロアルコールをアミノアルコールに化学的に還元することを含んでなる。アミンへのニトロ化合物の化学的還元は公知であり、種々の技術が“Comprehensive Chemical Transformations”、Richard C.Larock編;VCH Publishers、1989年、第411〜415頁に記載されている。水素化触媒の存在下での水素化が好ましい。
のオキサゾリジンの製造のためのプロセスが提供される。この態様のプロセスは、(a)前記のようにして製造された、式(III)のアミノアルコールを用意し、そして(b)式(III)のアミノアルコールをホルムアルデヒドと反応させることを含んでなる。
のN−アルキルヒドロキシルアミンの製造のためのプロセスが提供される。この態様のプロセスは、(a)前記のようにして製造された、式(I)のニトロ化炭化水素を用意し、(b)このニトロ化炭化水素をヒドロキシルアミンに化学的に還元することを含んでなる。ヒドロキシルアミンへのニトロ化合物の化学的還元は公知であり、種々の技術を使用することができる。ニトロアルカンからヒドロキシルアミンを製造するために使用される化学的還元剤の例には、ヨウ化サマリウム、Zn/NH4Cl、アルミニウムアマルガム及び水素化アルミニウムリチウムが含まれる。水素化触媒の存在下でニトロ化炭化水素を部分的に水素化することが、好ましい技術である。
のN−アルキル化アミノアルコールを生成することができる。式VIの化合物は、例えば中和剤、分散剤及びポリウレタン触媒としての用途を見出す。この例に従った好ましいアルキル化化合物は1−ヒドロキシメチル−1−(N,N−ジメチルアミノ)シクロヘキサンである。
のものである。
R10がH又は直鎖状C1〜C8アルキルであるとき、R9及びR10は、それらが結合している炭素と一緒に、直鎖状C5〜C18アルキル鎖を形成し、
R10がCH2OHであるとき、R9は直鎖状C12〜C16アルキルであり、そして
この化合物は2−ニトロ−1−ヘキサノール、2−ニトロ−1−ヘプタノール、2−ニトロ−1−オクタノール、2−メチル−2−ニトロ−1−ヘプタノール又は2−ニトロ−1−ドデカノールではない)
のニトロアルコールを提供する。
R12がH又は直鎖状C1〜C8アルキルであるとき、R11及びR12は、それらが結合している炭素と一緒に、直鎖状C6〜C18アルキル鎖を形成し、
R12が、CH2OHであるとき、R11は直鎖状C7〜C17アルキルであり、そして
この化合物は2−アミノ−1−ヘプタノール、2−アミノ−2−メチル−1−ヘキサノール、2−アミノ−1−オクタノール、2−アミノ−2−エチル−1−ヘキサノール、2−アミノ−1−ノナノール、2−アミノ−2−メチル−1−オクタノール、2−アミノ−1−デカノール、2−アミノ−2−オクチル−1,3−プロパンジオール、2−アミノ−2−ブチル−1−ヘキサノール、2−アミノ−1−ウンデカノール、2−アミノ−1−ドデカノール、2−アミノ−2−デシル−1,3−プロパンジオール、2−アミノ−1−トリデカノール、2−アミノ−2−メチル−1−ドデカノール、2−アミノ−1−テトラデカノール、2−アミノ−2−ドデシル−1,3−プロパンジオール、2−アミノ−2−メチル−1−トリデカノール、2−アミノ−1−ペンタデカノール、2−アミノ−2−トリデシル−1,3−プロパンジオール、2−アミノ−1−ヘキサデカノール、2−アミノ−2−テトラデシル−1,3−プロパンジオール、2−アミノ−2−メチル−1−ペンタデカノール、2−アミノ−2−ヘキシル−1−デカノール、2−アミノ−1−ヘプタデカノール、2−アミノ−2−ペンタデシル−1,3−プロパンジオール、2−アミノ−1−オクタデカノール又は2−アミノ−2−ヘキサデシル−1,3−プロパンジオールではない)
のアミノアルコールを提供する。
のオキサゾリジンを提供する。
本発明の種々の面を、研究所規模の反応器を使用して示す。この反応器は、反応器の長さに沿った温度プロフィールを決定するために、反応器の中心を軸的に下方に配置されたサーモウェルを有する、単一管シェル・アンド・チューブ型熱交換器である。この反応器は、長さが46インチで、1/2インチ外径(0.37インチ内径)2型チタンプロセスチューブ及び1/8インチ外径(0.093インチ内径)2型チタンサーモウェルを有する、1.25インチ外径304ステンレススチールであるシェルを有する。温度プロフィール測定のために、非常に微細な可動性サーモカップルを、サーモウェルの中に挿入する。このサーモウェルは取り除くことができ、反応器に充填物を充填することができる。この反応器を垂直に装着する。硝酸及び炭化水素反応剤流を、Swagelok“T”内で室温で混合し、その後、反応器の中に入れる。使用する熱油を、反応剤に対して向流で、反応器シェルに供給する。反応器排出液を、冷却剤として水道水を使用してシェル・アンド・チューブ型熱交換器内で冷却する。次いで、この排出液を加圧を除き、気体及び液体を集め、測定し、分析する。
1−ニトロオクタンの製造
この実施例は1−ニトロアルカンの製造のための代替手順の例示である。
2−メチル−2−ニトロ−1−ブタノールの製造
2リットルの三つ口フラスコに、機械式攪拌機、窒素バブラーを有する還流凝縮器、添加漏斗並びに加熱マントル及びサーモカップルを有する温度制御器を取り付ける。このフラスコに、ホルムアルデヒド水溶液(420mL、37%活性、5.64モル)及びトリエチルアミン触媒4mLを装入する。添加漏斗に、2−ニトロブタン(554.1g、5.37モル)を装入する。2−ニトロブタンを、ホルムアルデヒド溶液に7時間かけて滴下により添加し、この溶液を窒素下で撹拌する。添加の間、反応物を40℃で維持する。全ての2−ニトロブタンを添加した後、濁った混合物を45℃に30分間加温し、次いで、加熱及び撹拌を一晩中止する。GC分析が、反応が未だ完結していないことを示す場合、追加の10.9gのホルムアルデヒド水溶液を添加し、この混合物を45℃で2.5時間撹拌する。室温にまで冷却すると、反応塊は、より小さい分離した水層を伴う油層に分離する。この油層を集め(1022.8g、理論量の97.9%)、GCは94.8%純度を示す。この油を、更に精製することなく使用する。
2−アミノ−2−メチル−1−ブタノールの製造
2リットルのパルオートクレーブに、メタノール(300mL)及びラネーニッケル触媒(R−3111グレード、26.5g湿潤重量)を装入する。この反応器を密閉し、窒素でパージし、続いて水素でパージし、次いで、625psiの水素圧力下で65℃にする。急速に撹拌しながら、水中の2−ニトロ−2−メチル−1−ブタノールの溶液(全溶液450g、活性71%)を、65℃/610psiの水素を維持しながら、1.5時間かけて添加する。添加が完結したとき、反応を、更に10分間続けさせ、続いて室温にまで冷却する。オートクレーブを排気し、開き、粗製生成物を真空濾過によって単離する。メタノール溶媒をロータリーエバポレーターで50℃/29インチ真空で除去し、続いて、同一条件下で、100mLのトルエンと共に水の最後の残部を共沸的に除去する。粗製のストリップした生成物の収量は、196.6g(理論量の79%)である。この生成物を、ステンレススチールメッシュを充填した分別カラムによって真空蒸留し、85〜86℃/15トールで沸騰する生成物を集める。GC分析は、無色透明油について97%より低い純度を示す。
3−オキサ−1−アザスピロ[4.5]デカンの製造
1−アミノ−シクロヘキシルメタノール(135g、1.05モル)及びメタノール(50mL)を含有する500mLのフラスコに、メチルホルムセル(methyl formcel)(メタノール/水中の55%ホルムアルデヒド53mL、1.06モル)を、1時間かけて滴下により添加する。添加の間に、撹拌したこの溶液を、室温から37℃までゆっくり加温する。添加が完結した後、この混合物を、室温で一晩撹拌する。ロータリーエバポレーターで、透明で、無色の反応混合物をストリップする(50℃/29インチ真空)。得られる油を、真空下で蒸留して、43℃/0.8トールの沸点を有する、透明無色流動性液体を得る。合計123.4gを集める(83%収率)。GC分析が、95.6%純度を示す。
フェノール樹脂硬化剤としてのオキサゾリジン誘導体の使用
DSC分析
DSC分析は、TA Instruments モデルQ100示差走査熱量計を使用して実施する。ノボラック樹脂での硬化剤をスクリーニングするための走査を、50cc/分の窒素流で、25℃から250℃までΔT=10℃/分で行う。高体積(100μL)アルミニウムパンを使用する。クリンプの前に、頂部に、小さい孔を押し抜く。最初の走査の後に、サンプルを室温にまで戻し冷却し、次いで、走査を再び行って、Tgデータを得る。
以下に、本発明及びその関連態様を列挙する。
態様1.下降流配置反応器を用意し、
炭化水素供給原料を、少なくとも約500psiの圧力及び約150〜約325℃の温度で、硝酸水溶液と反応させ、そして
生成したニトロ化化合物を回収する
ことを含んでなり、前記硝酸水溶液が10〜50重量%溶液である炭化水素の選択的ニトロ化プロセス。
態様2.前記硝酸水溶液が15〜40重量%溶液である態様1に記載のプロセス。
態様3.前記硝酸水溶液が18〜35重量%溶液である、態様1又は2に記載のプロセス。
態様4.炭化水素供給原料の硝酸に対するモル比が少なくとも約1.2:1である態様1〜3に記載のプロセス。
態様5.前記温度が200℃又はそれ以上である態様1〜4に記載のプロセス。
態様6.前記温度が290℃又はそれ以上である態様1〜5に記載のプロセス。
態様7.前記反応を、充填反応器内で、実施する態様1〜6に記載のプロセス。
態様8.前記反応を、非充填反応器内で、実施する態様1〜6に記載のプロセス。
態様9.前記炭化水素供給原料がアルカン、アリールアルカン、ナフチルアルカン及びビアリールアルカンから選択される態様1〜8に記載のプロセス。
態様10.前記ニトロ化化合物が、式(I):
の化合物である態様1〜9に記載のプロセス。
態様11.式II:
のニトロアルコールの製造プロセスであって、
(a)態様10の記載に従って製造された、式(I)(式中、R y はHである)のニトロ化炭化水素を用意し、そして
(b)前記ニトロ化炭化水素を、式:R 5 −C(=O)−Hのアルデヒドと、アルカリ性触媒の存在下に、縮合させて、式(II)のニトロアルコールを提供する
ことを含んでなるプロセス。
態様12.式(III):
のアミノアルコールの製造プロセスであって、
(a)態様11に従って製造された、式(II)のニトロアルコールを用意し、そして
(b)前記ニトロアルコールを化学的に還元して、式(III)のアミノアルコールを提供する
ことを含んでなるプロセス。
態様13.式(IV):
のオキサゾリジンの製造プロセスであって、
(a)態様12に従って製造された、式(III)のアミノアルコールを用意し、そして
(b)式(III)のアミノアルコールをホルムアルデヒドと反応させて、式(IV)のオキサゾリジンを提供する
ことを含んでなるプロセス。
態様14.式(V):
のN−アルキルヒドロキシルアミンの製造プロセスであって、
(a)態様10に従って製造された、式(I)のニトロ化炭化水素を用意し、
(b)前記ニトロ化炭化水素を化学的に還元して、式(V)のN−アルキルヒドロキシルアミンを提供する
ことを含んでなるプロセス。
態様15.式VI:
の化合物の製造プロセスであって、
(a)態様12に従って製造された、式(III)のアミノアルコールを用意し、そして
(b)前記アミノアルコールを、アルデヒド、水素及び水素化触媒の存在下に、還元的にアルキル化して、式VIの化合物を提供する
ことを含んでなるプロセス。
態様16.式I−1:
の化合物。
態様17.3−ニトロデカン、4−ニトロデカン、5−ニトロデカン、4−ニトロトリデカン、5−ニトロトリデカン、7−ニトロトリデカン、2−ニトロテトラデカン、3−ニトロテトラデカン、4−ニトロテトラデカン、5−ニトロテトラデカン、6−ニトロテトラデカン、7−ニトロテトラデカン、2−ニトロペンタデカン、3−ニトロペンタデカン、4−ニトロペンタデカン、5−ニトロペンタデカン、6−ニトロペンタデカン、7−ニトロペンタデカン、8−ニトロペンタデカン、3−ニトロヘキサデカン、4−ニトロヘキサデカン、5−ニトロヘキサデカン、6−ニトロヘキサデカン、7−ニトロヘキサデカン、8−ニトロヘキサデカン、2−ニトロヘプタデカン、3−ニトロヘプタデカン、4−ニトロヘプタデカン、5−ニトロヘプタデカン、6−ニトロヘプタデカン、7−ニトロヘプタデカン、8−ニトロヘプタデカン、9−ニトロヘプタデカン、3−ニトロオクタデカン、4−ニトロオクタデカン、5−ニトロオクタデカン、6−ニトロオクタデカン、7−ニトロオクタデカン、8−ニトロオクタデカン及び9−ニトロオクタデカンからなる群から選択される態様16に記載の化合物。
態様18.式II−1:
R 10 がH又は直鎖状C 1 〜C 8 アルキルであるとき、R 9 及びR 10 は、それらが結合している炭素と一緒に、直鎖状C 5 〜C 18 アルキル鎖を形成し、
R 10 がCH 2 OHであるとき、R 9 は直鎖状C 12 〜C 16 アルキルであり、そして
当該化合物は2−ニトロ−1−ヘキサノール、2−ニトロ−1−ヘプタノール、2−ニトロ−1−オクタノール、2−メチル−2−ニトロ−1−ヘプタノール又は2−ニトロ−1−ドデカノールではない)
の化合物。
態様19.2−メチル−2−ニトロ−1−ペンタノール、2−エチル−2−ニトロ−1−ブタノール、2−メチル−2−ニトロ−1−ヘキサノール、2−エチル−2−ニトロ−1−ペンタノール、2−エチル−2−ニトロ−1−ヘキサノール、2−ニトロ−2−プロピル−1−ペンタノール、2−ニトロ−1−ノナノール、2−メチル−2−ニトロ−1−オクタノール、2−エチル−2−ニトロ−1−ヘプタノール、2−ニトロ−2−プロピル−1−ヘキサノール、2−ニトロ−1−デカノール、2−メチル−2−ニトロ−1−ノナノール、2−エチル−2−ニトロ−1−オクタノール、2−ニトロ−2−プロピル−1−ヘプタノール、2−ブチル−2−ニトロ−1−ヘキサノール、2−ニトロ−1−ウンデカノール、2−メチル−2−ニトロ−1−デカノール、2−エチル−2−ニトロ−1−ノナノール、2−プロピル−2−ニトロ−1−オクタノール、2−ブチル−2−ニトロ−1−ヘプタノール、2−メチル−2−ニトロ−1−ウンデカノール、2−エチル−2−ニトロ−1−デカノール、2−プロピル−2−ニトロ−1−ノナノール、2−ブチル−2−ニトロ−1−オクタノール、2−ペンチル−2−ニトロ−1−ヘプタノール、2−ニトロ−1−トリデカノール、2−メチル−2−ニトロ−1−ドデカノール、2−エチル−2−ニトロ−1−ウンデカノール、2−プロピル−2−ニトロ−1−デカノール、2−ブチル−2−ニトロ−1−ノナノール、2−ペンチル−2−ニトロ−1−オクタノール、2−ニトロ−1−テトラデカノール、2−ヒドロキシメチル−2−ニトロ−1−テトラデカノール、2−メチル−2−ニトロ−1−トリデカノール、2−エチル−2−ニトロ−1−ドデカノール、2−プロピル−2−ニトロ−1−ウンデカノール、2−ブチル−2−ニトロ−1−デカノール、2−ペンチル−2−ニトロ−1−ノナノール、2−ヘキシル−2−ニトロ−1−オクタノール、2−ニトロ−1−ペンタデカノール、2−ヒドロキシメチル−2−ニトロ−1−ペンタデカノール、2−メチル−2−ニトロ−1−テトラデカノール、2−エチル−2−ニトロ−1−トリデカノール、2−プロピル−2−ニトロ−1−ドデカノール、2−ブチル−2−ニトロ−1−ウンデカノール、2−ペンチル−2−ニトロ−1−デカノール、2−ヘキシル−2−ニトロ−1−ノナノール、2−ヘプチル−2−ニトロ−1−オクタノール、2−ニトロ−1−ヘキサデカノール、2−ヒドロキシメチル−2−ニトロ−1−ヘキサデカノール、2−メチル−2−ニトロ−1−ペンタデカノール、2−エチル−2−ニトロ−1−テトラデカノール、2−プロピル−2−ニトロ−1−トリデカノール、2−ブチル−2−ニトロ−1−ドデカノール、2−ペンチル−2−ニトロ−1−ウンデカノール、2−ヘキシル−2−ニトロ−1−デカノール、2−ヘプチル−2−ニトロ−1−ノナノール、2−ニトロ−1−ヘプタデカノール、2−ヒドロキシメチル−2−ニトロ−1−ヘプタデカノール、2−メチル−2−ニトロ−1−ヘキサデカノール、2−エチル−2−ニトロ−1−ペンタデカノール、2−プロピル−2−ニトロ−1−テトラデカノール、2−ブチル−2−ニトロ−1−トリデカノール、2−ペンチル−2−ニトロ−ドデカノール、2−ヘキシル−2−ニトロ−1−ウンデカノール、2−ヘプチル−2−ニトロ−1−デカノール、2−ニトロ−1−オクタデカノール、2−ヒドロキシメチル−2−ニトロ−1−オクタデカノール、2−メチル−2−ニトロ−1−ヘプタデカノール、2−エチル−2−ニトロ−1−ヘキサデカノール、2−プロピル−2−ニトロ−1−ペンタデカノール、2−ブチル−2−ニトロ−1−テトラデカノール、2−ペンチル−2−ニトロ−1−トリデカノール、2−ヘキシル−2−ニトロ−1−ドデカノール、2−ヘプチル−2−ニトロ−1−ウンデカノール、2−オクチル−2−ニトロ−1−デカノール、2−ニトロ−1−ノナデカノール、2−メチル−2−ニトロ−1−オクタデカノール、2−エチル−2−ニトロ−1−ヘプタデカノール、2−プロピル−2−ニトロ−1−ヘキサデカノール、2−ブチル−2−ニトロ−1−ペンタデカノール、2−ペンチル−2−ニトロ−1−テトラデカノール、2−ヘキシル−2−ニトロ−1−トリデカノール、2−ヘプチル−2−ニトロ−1−ドデカノール、2−オクチル−2−ニトロ−1−ウンデカノール及び1−ヒドロキシメチル−1−ニトロシクロオクタンからなる群から選択される、態様18に記載の化合物。
態様20.式III−1:
R 12 がH又は直鎖状C 1 〜C 8 アルキルであるとき、R 11 及びR 12 は、それらが結合している炭素と一緒に、直鎖状C 6 〜C 18 アルキル鎖を形成し、
R 12 がCH 2 OHであるとき、R 11 は直鎖状C 7 〜C 17 アルキルであり、そして
前記化合物は2−アミノ−1−ヘプタノール、2−アミノ−2−メチル−1−ヘキサノール、2−アミノ−1−オクタノール、2−アミノ−2−エチル−1−ヘキサノール、2−アミノ−1−ノナノール、2−アミノ−2−メチル−1−オクタノール、2−アミノ−1−デカノール、2−アミノ−2−オクチル−1,3−プロパンジオール、2−アミノ−2−ブチル−1−ヘキサノール、2−アミノ−1−ウンデカノール、2−アミノ−1−ドデカノール、2−アミノ−2−デシル−1,3−プロパンジオール、2−アミノ−1−トリデカノール、2−アミノ−2−メチル−1−ドデカノール、2−アミノ−1−テトラデカノール、2−アミノ−2−ドデシル−1,3−プロパンジオール、2−アミノ−2−メチル−1−トリデカノール、2−アミノ−1−ペンタデカノール、2−アミノ−2−トリデシル−1,3−プロパンジオール、2−アミノ−1−ヘキサデカノール、2−アミノ−2−テトラデシル−1,3−プロパンジオール、2−アミノ−2−メチル−1−ペンタデカノール、2−アミノ−2−ヘキシル−1−デカノール、2−アミノ−1−ヘプタデカノール、2−アミノ−2−ペンタデシル−1,3−プロパンジオール、2−アミノ−1−オクタデカノール又は2−アミノ−2−ヘキサデシル−1,3−プロパンジオールではない)
の化合物。
態様21.2−アミノ−2−エチル−1−ペンタノール、2−アミノ−2−メチル−1−ヘプタノール、2−アミノ−2−プロピル−1−ペンタノール、2−アミノ−2−ヘプチル−1,3−プロパンジオール、2−アミノ−2−エチル−1−ヘプタノール、2−アミノ−2−プロピル−1−ヘキサノール、2−アミノ−2−メチル−1−ノナノール、2−アミノ−2−エチル−1−オクタノール、2−アミノ−2−プロピル−1−ヘプタノール、2−アミノ−2−ノニル−1,3−プロパンジオール、2−アミノ−2−メチル−1−デカノール、2−アミノ−2−エチル−1−ノナノール、2−アミノ−2−プロピル−1−オクタノール、2−アミノ−2−ブチル−1−ヘプタノール、2−アミノ−2−メチル−1−ウンデカノール、2−アミノ−2−エチル−1−デカノール、2−アミノ−2−プロピル−1−ノナノール、2−アミノ−2−ブチル−1−オクタノール、2−アミノ−2−ペンチル−1−ヘプタノール、2−アミノ−2−ウンデシル−1,3−プロパンジオール、2−アミノ−2−エチル−1−ウンデカノール、2−アミノ−2−プロピル−1−デカノール、2−アミノ−2−ブチル−1−ノナノール、2−アミノ−2−ペンチル−1−オクタノール、2−アミノ−2−エチル−1−ドデカノール、2−アミノ−2−プロピル−1−ウンデカノール、2−アミノ−2−ブチル−1−デカノール、2−アミノ−2−ペンチル−1−ノナノール、2−アミノ−2−ヘキシル−1−オクタノール、2−アミノ−2−メチル−1−テトラデカノール、2−アミノ−2−エチル−1−トリデカノール、2−アミノ−2−プロピル−1−ドデカノール、2−アミノ−2−ブチル−1−ウンデカノール、2−アミノ−2−ペンチル−1−デカノール、2−アミノ−2−ヘキシル−1−ノナノール、2−アミノ−2−エチル−1−テトラデカノール、2−アミノ−2−プロピル−1−トリデカノール、2−アミノ−2−ブチル−1−ドデカノール、2−アミノ−2−ペンチル−1−ウンデカノール、2−アミノ−2−ヘプチル−1−ノナノール、2−アミノ−2−メチル−1−ヘキサデカノール、2−アミノ−2−エチル−1−ペンタデカノール、2−アミノ−2−プロピル−1−テトラデカノール、2−アミノ−2−ブチル−1−トリデカノール、2−アミノ−2−ペンチル−1−ドデカノール、2−アミノ−2−ヘキシル−1−ウンデカノール、2−アミノ−2−ヘプチル−1−デカノール、2−アミノ−2−メチル−1−ヘプタデカノール、2−アミノ−2−エチル−1−ヘキサデカノール、2−アミノ−2−プロピル−1−ペンタデカノール、2−アミノ−2−ブチル−1−テトラデカノール、2−アミノ−2−ペンチル−1−トリデカノール、2−アミノ−2−ヘキシル−1−ドデカノール、2−アミノ−2−ヘプチル−1−ウンデカノール、2−アミノ−2−オクチル−1−デカノール、2−アミノ−1−ノナデカノール、2−アミノ−2−ヘプタデシル−1,3−プロパンジオール、2−アミノ−2−メチル−1−オクタデカノール、2−アミノ−2−エチル−1−ヘプタデカノール、2−アミノ−2−プロピル−1−ヘキサデカノール、2−アミノ−2−ブチル−1−ペンタデカノール、2−アミノ−2−ペンチル−1−テトラデカノール、2−アミノ−2−ヘキシル−1−トリデカノール、2−アミノ−2−ヘプチル−1−ドデカノール、2−アミノ−2−オクチル−1−ウンデカノール、1−ヒドロキシメチル−1−アミノシクロノナン、1−ヒドロキシメチル−1−アミノシクロデカン及び1−ヒドロキシメチル−1−アミノシクロウンデカンからなる群から選択される態様20に記載の化合物。
態様22.式IV−1:
の化合物。
態様23.4−プロピル−1−オキサ−3−アザシクロペンタン、4−エチル−4−メチル−1−オキサ−3−アザシクロペンタン、4−ブチル−1−オキサ−3−アザシクロペンタン、5−ブチル−1−アザ−3,7−ジオキサビシクロ[3.3.0]オクタン、4−プロピル−4−メチル−1−オキサ−3−アザシクロペンタン、4−ペンチル−1−オキサ−3−アザシクロペンタン、5−ペンチル−1−アザ−3,7−ジオキサビシクロ[3.3.0]オクタン、4−ブチル−4−メチル−1−オキサ−3−アザシクロペンタン、4−エチル−4−プロピル−1−オキサ−3−アザシクロペンタン、4−ヘキシル−1−オキサ−3−アザシクロペンタン、5−ヘキシル−1−アザ−3,7−ジオキサビシクロ[3.3.0]オクタン、4−メチル−4−プロピル−1−オキサ−3−アザシクロペンタン、4,4−ジプロピル−1−オキサ−3−アザシクロペンタン、4−ブチル−4−エチル−1−オキサ−3−アザシクロペンタン、4−ヘプチル−1−オキサ−3−アザシクロペンタン、5−ヘプチル−1−アザ−3,7−ジオキサビシクロ[3.3.0]オクタン、4−ヘキシル−4−メチル−1−オキサ−3−アザシクロペンタン、4−エチル−4−ペンチル−1−オキサ−3−アザシクロペンタン、4−ブチル−4−プロピル−1−オキサ−3−アザシクロペンタン、4−オクチル−1−オキサ−3−アザシクロペンタン、5−オクチル−1−アザ−3,7−ジオキサビシクロ[3.3.0]オクタン、4−ヘプチル−4−メチル−1−オキサ−3−アザシクロペンタン、4−エチル−4−ヘキシル−1−オキサ−3−アザシクロペンタン、4−ペンチル−4−プロピル−1−オキサ−3−アザシクロペンタン、4,4−ジブチル−1−オキサ−3−アザシクロペンタン、4−ノニル−1−オキサ−3−アザシクロペンタン、5−ノニル−1−アザ−3,7−ジオキサビシクロ[3.3.0]オクタン、4−メチル−4−オクチル−1−オキサ−3−アザシクロペンタン、4−エチル−4−ヘプチル−1−オキサ−3−アザシクロペンタン、4−ヘキシル−4−プロピル−1−オキサ−3−アザシクロペンタン、4−ブチル−4−ペンチル−1−オキサ−3−アザシクロペンタン、4−デシル−1−オキサ−3−アザシクロペンタン、5−デシル−1−アザ−3,7−ジオキサビシクロ[3.3.0]オクタン、4−メチル−4−ノニル−1−オキサ−3−アザシクロペンタン、4−ヘプチル−4−プロピル−1−オキサ−3−アザシクロペンタン、4−エチル−4−オクチル−1−オキサ−3−アザシクロペンタン、4−ブチル−4−ヘキシル−1−オキサ−3−アザシクロペンタン、4,4−ジペンチル−1−オキサ−3−アザシクロペンタン、4−ウンデシル−1−オキサ−3−アザシクロペンタン、5−ウンデシル−1−アザ−3,7−ジオキサビシクロ[3.3.0]オクタン、4−デシル−4−メチル−1−オキサ−3−アザシクロペンタン、4−エチル−4−ノニル−1−オキサ−3−アザシクロペンタン、4−オクチル−4−プロピル−1−オキサ−3−アザシクロペンタン、4−ブチル−4−ヘプチル−1−オキサ−3−アザシクロペンタン、4−ヘキシル−4−ペンチル−1−オキサ−3−アザシクロペンタン、4−ドデシル−1−オキサ−3−アザシクロペンタン、5−ドデシル−1−アザ−3,7−ジオキサビシクロ[3.3.0]オクタン、4−メチル−4−ウンデシル−1−オキサ−3−アザシクロペンタン、4−デシル−4−エチル−1−オキサ−3−アザシクロペンタン、4−ノニル−4−プロピル−1−オキサ−3−アザシクロペンタン、4−ブチル−4−オクチル−1−オキサ−3−アザシクロペンタン、4−ヘプチル−4−ペンチル−1−オキサ−3−アザシクロペンタン、4,4−ジヘキシル−1−オキサ−3−アザシクロペンタン、4−トリデシル−1−オキサ−3−アザシクロペンタン、5−トリデシル−1−アザ−3,7−ジオキサビシクロ[3.3.0]オクタン、4−ドデシル−4−メチル−1−オキサ−3−アザシクロペンタン、4−エチル−4−ウンデシル−1−オキサ−3−アザシクロペンタン、4−デシル−4−プロピル−1−オキサ−3−アザシクロペンタン、4−ブチル−4−ノニル−1−オキサ−3−アザシクロペンタン、4−オクチル−4−ペンチル−1−オキサ−3−アザシクロペンタン、4−ヘプチル−4−ヘキシル−1−オキサ−3−アザシクロペンタン、4−テトラデシル−1−オキサ−3−アザシクロペンタン、5−テトラデシル−1−アザ−3,7−ジオキサビシクロ[3.3.0]オクタン、4−メチル−4−トリデシル−1−オキサ−3−アザシクロペンタン、4−ドデシル−4−エチル−1−オキサ−3−アザシクロペンタン、4−プロピル−4−ウンデシル−1−オキサ−3−アザシクロペンタン、4−ブチル−4−デシル−1−オキサ−3−アザシクロペンタン、4−ノニル−4−ペンチル−1−オキサ−3−アザシクロペンタン、4−ヘキシル−4−オクチル−1−オキサ−3−アザシクロペンタン、4,4−ジヘプチル−1−オキサ−3−アザシクロペンタン、4−ペンタデシル−1−オキサ−3−アザシクロペンタン、5−ペンタデシル−1−アザ−3,7−ジオキサビシクロ[3.3.0]オクタン、4−メチル−4−テトラデシル−1−オキサ−3−アザシクロペンタン、4−エチル−4−トリデシル−1−オキサ−3−アザシクロペンタン、4−ドデシル−4−プロピル−1−オキサ−3−アザシクロペンタン、4−ブチル−4−ウンデシル−1−オキサ−3−アザシクロペンタン、4−デシル−4−ペンチル−1−オキサ−3−アザシクロペンタン、4−ヘキシル−4−ノニル−1−オキサ−3−アザシクロペンタン、4−ヘプチル−4−オクチル−1−オキサ−3−アザシクロペンタン、4−ヘキサデシル−1−オキサ−3−アザシクロペンタン、5−ヘキサデシル−1−アザ−3,7−ジオキサビシクロ[3.3.0]オクタン、4−メチル−4−ペンタデシル−1−オキサ−3−アザシクロペンタン、4−エチル−4−テトラデシル−1−オキサ−3−アザシクロペンタン、4−プロピル−4−トリデシル−1−オキサ−3−アザシクロペンタン、4−ブチル−4−ドデシル−1−オキサ−3−アザシクロペンタン、4−ペンチル−4−ウンデシル−1−オキサ−3−アザシクロペンタン、4−デシル−4−ヘキシル−1−オキサ−3−アザシクロペンタン、4−ヘプチル−4−ノニル−1−オキサ−3−アザシクロペンタン、4,4−ジオクチル−1−オキサ−3−アザシクロペンタン、4−ヘプタデシル−1−オキサ−3−アザシクロペンタン、5−ヘプタデシル−1−アザ−3,7−ジオキサビシクロ[3.3.0]オクタン、4−ヘキサデシル−4−メチル−1−オキサ−3−アザシクロペンタン、4−エチル−4−ペンタデシル−1−オキサ−3−アザシクロペンタン、4−プロピル−4−テトラデシル−1−オキサ−3−アザシクロペンタン、4−ブチル−4−トリデシル−1−オキサ−3−アザシクロペンタン、4−ドデシル−4−ペンチル−1−オキサ−3−アザシクロペンタン、4−ヘキシル−4−ウンデシル−1−オキサ−3−アザシクロペンタン、4−デシル−4−ヘプチル−1−オキサ−3−アザシクロペンタン及び4−オクチル−4−ノニル−1−オキサ−3−アザシクロペンタンからなる群から選択される態様22に記載の化合物。
態様24.2−(ヒドロキシルアミノ)ヘキサン、3−(ヒドロキシルアミノ)ヘキサン、2−(ヒドロキシルアミノ)オクタン及び3−(ヒドロキシルアミノ)オクタンからなる群から選択される化合物。
態様25.式(III):
のアミノアルコールの、ペイント及びコーティング中の中和剤若しくは分散剤としての、石油精製運転及び天然ガスプロセッシングに於けるCO 2 若しくはH 2 Sスカベンジャーとしての又はエポキシ若しくはポリウレタン用途に於ける触媒若しくは硬化剤としての使用。
態様26.ペイント及びコーティング中の中和剤若しくは分散剤としての、石油精製運転及び天然ガスプロセッシングに於けるCO 2 若しくはH 2 Sスカベンジャーとしての又はエポキシ若しくはポリウレタン用途に於ける触媒若しくは硬化剤としての、態様20に記載のアミノアルコールの使用。
態様27.式(IV):
のオキサゾリジンの、殺生物剤としての又は例えばフェノール性ノボラック樹脂用の硬化剤としての使用。
態様28.殺生物剤としての又は例えばフェノール性ノボラック樹脂用の硬化剤としての、態様22に記載のオキサゾリジンの使用。
態様29.式(V):
のヒドロキシルアミンの、ラジカルスカベンジャーとしての使用。
態様30.ラジカルスカベンジャーとしての、態様24に記載の化合物の使用。
態様31.燃料中の安定剤及び/若しくは腐食制御剤、モノマーの安定剤又はゴム重合に於ける連鎖停止剤としての、態様29〜30に記載の使用。
Claims (11)
- 下降流配置反応器を用意し、
炭化水素供給原料を、少なくとも500psi(3447.4kPa)の圧力及び150〜325℃の温度で、硝酸水溶液と反応させ、そして
生成したニトロ化化合物を回収する
ことを含んでなり、前記硝酸水溶液が10〜35重量%溶液である、炭化水素の選択的ニトロ化プロセス。 - 前記硝酸水溶液が18〜35重量%溶液である、請求項1に記載のプロセス。
- 炭化水素供給原料の硝酸に対するモル比が少なくとも1.2:1である請求項1又は2に記載のプロセス。
- 前記温度が200℃又はそれ以上である請求項1〜3のいずれか1項に記載のプロセス。
- 前記炭化水素供給原料がアルカン、アリールアルカン、ナフチルアルカン及びビアリールアルカンから選択される請求項1〜4のいずれか1項に記載のプロセス。
- 式II:
のニトロアルコールの製造プロセスであって、
(a)請求項6の記載に従って、式(I)(式中、RyはHである)のニトロ化炭化水素を製造し、そして
(b)前記ニトロ化炭化水素を、式:R5−C(=O)−Hのアルデヒドと、アルカリ性触媒の存在下に、縮合させて、式(II)のニトロアルコールを提供する
ことを含んでなるプロセス。 - 式(III):
のアミノアルコールの製造プロセスであって、
(a)請求項7に従って、式(II)のニトロアルコールを製造し、そして
(b)前記ニトロアルコールを化学的に還元して、式(III)のアミノアルコールを提供する
ことを含んでなるプロセス。 - 式(IV):
のオキサゾリジンの製造プロセスであって、
(a)請求項8に従って、式(III)のアミノアルコールを製造し、そして
(b)式(III)のアミノアルコールをホルムアルデヒドと反応させて、式(IV)のオキサゾリジンを提供する
ことを含んでなるプロセス。 - 式(V):
のN−アルキルヒドロキシルアミンの製造プロセスであって、
(a)請求項6に従って、式(I)のニトロ化炭化水素を製造し、
(b)前記ニトロ化炭化水素を化学的に還元して、式(V)のN−アルキルヒドロキシルアミンを提供する
ことを含んでなるプロセス。 - 式VI:
の化合物の製造プロセスであって、
(a)請求項8に従って、式(III)のアミノアルコールを製造し、そして
(b)前記アミノアルコールを、アルデヒド、水素及び水素化触媒の存在下に、還元的にアルキル化して、式VIの化合物を提供する
ことを含んでなるプロセス。
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