JP5070208B2 - ヒドロホルミル化方法 - Google Patents
ヒドロホルミル化方法 Download PDFInfo
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- JP5070208B2 JP5070208B2 JP2008518856A JP2008518856A JP5070208B2 JP 5070208 B2 JP5070208 B2 JP 5070208B2 JP 2008518856 A JP2008518856 A JP 2008518856A JP 2008518856 A JP2008518856 A JP 2008518856A JP 5070208 B2 JP5070208 B2 JP 5070208B2
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- 238000000034 method Methods 0.000 title claims abstract description 94
- 238000007037 hydroformylation reaction Methods 0.000 title claims abstract description 66
- 238000006243 chemical reaction Methods 0.000 claims abstract description 196
- 239000003054 catalyst Substances 0.000 claims abstract description 75
- 150000001875 compounds Chemical class 0.000 claims abstract description 51
- 239000000203 mixture Substances 0.000 claims abstract description 34
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 24
- 150000001868 cobalt Chemical class 0.000 claims abstract description 22
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 17
- 239000001257 hydrogen Substances 0.000 claims abstract description 17
- 229910017052 cobalt Inorganic materials 0.000 claims description 51
- 239000010941 cobalt Substances 0.000 claims description 51
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 51
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 29
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 26
- 239000003446 ligand Substances 0.000 claims description 24
- -1 olefin compound Chemical class 0.000 claims description 23
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 20
- 239000002994 raw material Substances 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 12
- 229910052698 phosphorus Inorganic materials 0.000 claims description 11
- 125000004437 phosphorous atom Chemical group 0.000 claims description 10
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 abstract description 15
- 150000001336 alkenes Chemical class 0.000 description 29
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 27
- 239000000047 product Substances 0.000 description 25
- 238000004519 manufacturing process Methods 0.000 description 18
- 150000001299 aldehydes Chemical class 0.000 description 17
- 150000001298 alcohols Chemical class 0.000 description 15
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 12
- 150000001721 carbon Chemical group 0.000 description 12
- 238000012360 testing method Methods 0.000 description 12
- 239000006227 byproduct Substances 0.000 description 11
- 239000012188 paraffin wax Substances 0.000 description 10
- 239000007795 chemical reaction product Substances 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- 125000000962 organic group Chemical group 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 150000001923 cyclic compounds Chemical class 0.000 description 4
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 238000006317 isomerization reaction Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 229910052703 rhodium Inorganic materials 0.000 description 2
- 239000010948 rhodium Substances 0.000 description 2
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Chemical group 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 125000001424 substituent group Chemical class 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 150000003624 transition metals Chemical class 0.000 description 2
- BCAUVGPOEXLTJD-UHFFFAOYSA-N (2-cyclohexyl-4,6-dinitrophenyl) acetate Chemical compound C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(OC(=O)C)=C1C1CCCCC1 BCAUVGPOEXLTJD-UHFFFAOYSA-N 0.000 description 1
- AHAREKHAZNPPMI-AATRIKPKSA-N (3e)-hexa-1,3-diene Chemical compound CC\C=C\C=C AHAREKHAZNPPMI-AATRIKPKSA-N 0.000 description 1
- ZITVKGIRQCDOSX-UHFFFAOYSA-N 1h-cyclopropa[a]naphthalene Chemical compound C1=CC=CC2=C3CC3=CC=C21 ZITVKGIRQCDOSX-UHFFFAOYSA-N 0.000 description 1
- MMEDJBFVJUFIDD-UHFFFAOYSA-N 2-[2-(carboxymethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC=C1CC(O)=O MMEDJBFVJUFIDD-UHFFFAOYSA-N 0.000 description 1
- ONIKNECPXCLUHT-UHFFFAOYSA-N 2-chlorobenzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1Cl ONIKNECPXCLUHT-UHFFFAOYSA-N 0.000 description 1
- DKPWQXOONAEKGH-UHFFFAOYSA-N 2-cyclononyl-1-icosylphosphonane Chemical class CCCCCCCCCCCCCCCCCCCCP1CCCCCCCC1C1CCCCCCCC1 DKPWQXOONAEKGH-UHFFFAOYSA-N 0.000 description 1
- BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical group CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 description 1
- IAXKTDPGBOOLGE-UHFFFAOYSA-N 4,7-dimethyl-9-phenyl-9-phosphabicyclo[4.2.1]nonane Chemical compound CC1CC2CCC(C)CC1P2C1=CC=CC=C1 IAXKTDPGBOOLGE-UHFFFAOYSA-N 0.000 description 1
- WUCWMUVIWKIXOA-UHFFFAOYSA-N 4,8-dimethyl-9-phenyl-9-phosphabicyclo[4.2.1]nonane Chemical compound CC1CC2CC(C)CCC1P2C1=CC=CC=C1 WUCWMUVIWKIXOA-UHFFFAOYSA-N 0.000 description 1
- LDZLXQFDGRCELX-UHFFFAOYSA-N 4-phenylbutan-1-ol Chemical compound OCCCCC1=CC=CC=C1 LDZLXQFDGRCELX-UHFFFAOYSA-N 0.000 description 1
- NHFRGTVSKOPUBK-UHFFFAOYSA-N 4-phenylbutanal Chemical compound O=CCCCC1=CC=CC=C1 NHFRGTVSKOPUBK-UHFFFAOYSA-N 0.000 description 1
- CCWGYOMWNDNDBQ-UHFFFAOYSA-N 9-(cycloocten-1-yl)-9-phosphabicyclo[4.2.1]nonane Chemical compound C1CC2CCCCC1P2C1=CCCCCCC1 CCWGYOMWNDNDBQ-UHFFFAOYSA-N 0.000 description 1
- QEYRAXDZGINFSO-UHFFFAOYSA-N 9-cyclohexyl-9-phosphabicyclo[4.2.1]nonane Chemical compound C1CC2CCCCC1P2C1CCCCC1 QEYRAXDZGINFSO-UHFFFAOYSA-N 0.000 description 1
- PFXVRTONFFJWOR-UHFFFAOYSA-N 9-hexyl-9-phosphabicyclo[3.3.1]nonane Chemical compound C1CCC2CCCC1P2CCCCCC PFXVRTONFFJWOR-UHFFFAOYSA-N 0.000 description 1
- KQFHBBUICBFQME-UHFFFAOYSA-N 9-hexyl-9-phosphabicyclo[4.2.1]nonane Chemical compound C1CCCC2CCC1P2CCCCCC KQFHBBUICBFQME-UHFFFAOYSA-N 0.000 description 1
- QBUBJAXSVUKLBJ-UHFFFAOYSA-N 9-icosyl-9-phosphabicyclo[3.3.1]nonane Chemical compound C1CCC2CCCC1P2CCCCCCCCCCCCCCCCCCCC QBUBJAXSVUKLBJ-UHFFFAOYSA-N 0.000 description 1
- UNOOEFGBOLKBFW-UHFFFAOYSA-N 9-icosyl-9-phosphabicyclo[4.2.1]nonane Chemical compound C1CCCC2CCC1P2CCCCCCCCCCCCCCCCCCCC UNOOEFGBOLKBFW-UHFFFAOYSA-N 0.000 description 1
- RHBPCOITPOBTBL-UHFFFAOYSA-N 9-octadecyl-9-phosphabicyclo[4.2.1]nonane Chemical compound C1CCCC2CCC1P2CCCCCCCCCCCCCCCCCC RHBPCOITPOBTBL-UHFFFAOYSA-N 0.000 description 1
- KBHRXCWOPXOJIP-UHFFFAOYSA-N 9-phenyl-9-phosphabicyclo[3.3.1]nonane Chemical compound C1CCC2CCCC1P2C1=CC=CC=C1 KBHRXCWOPXOJIP-UHFFFAOYSA-N 0.000 description 1
- HXWCOMBZFBADSS-UHFFFAOYSA-N 9-phenyl-9-phosphabicyclo[4.2.1]nonane Chemical compound C1CC2CCCCC1P2C1=CC=CC=C1 HXWCOMBZFBADSS-UHFFFAOYSA-N 0.000 description 1
- HJRIAAMPPMMJNL-UHFFFAOYSA-N 9-triacontyl-9-phosphabicyclo[4.2.1]nonane Chemical compound C1CCCC2CCC1P2CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC HJRIAAMPPMMJNL-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- IUHFWCGCSVTMPG-UHFFFAOYSA-N [C].[C] Chemical class [C].[C] IUHFWCGCSVTMPG-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001334 alicyclic compounds Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 230000003113 alkalizing effect Effects 0.000 description 1
- 125000005530 alkylenedioxy group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 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
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- UMYVESYOFCWRIW-UHFFFAOYSA-N cobalt;methanone Chemical class O=C=[Co] UMYVESYOFCWRIW-UHFFFAOYSA-N 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- ZXIJMRYMVAMXQP-UHFFFAOYSA-N cycloheptene Chemical compound C1CCC=CCC1 ZXIJMRYMVAMXQP-UHFFFAOYSA-N 0.000 description 1
- VELDYOPRLMJFIK-UHFFFAOYSA-N cyclopentanecarbaldehyde Chemical compound O=CC1CCCC1 VELDYOPRLMJFIK-UHFFFAOYSA-N 0.000 description 1
- ISQVBYGGNVVVHB-UHFFFAOYSA-N cyclopentylmethanol Chemical compound OCC1CCCC1 ISQVBYGGNVVVHB-UHFFFAOYSA-N 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- MQIKJSYMMJWAMP-UHFFFAOYSA-N dicobalt octacarbonyl Chemical group [Co+2].[Co+2].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-] MQIKJSYMMJWAMP-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000012527 feed solution Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 150000004673 fluoride salts Chemical class 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000002815 homogeneous catalyst Substances 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 description 1
- IRUCBBFNLDIMIK-UHFFFAOYSA-N oct-4-ene Chemical compound CCCC=CCCC IRUCBBFNLDIMIK-UHFFFAOYSA-N 0.000 description 1
- 125000005474 octanoate group Chemical class 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229930015698 phenylpropene Natural products 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 239000011555 saturated liquid Substances 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000013517 stratification Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000004711 α-olefin Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/49—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
- C07C45/50—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/16—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxo-reaction combined with reduction
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Description
本発明によれば、有機ホスフィン修飾されたコバルトヒドロホルミル化触媒存在下、少なくとも1つのオレフィン性炭素−炭素結合を有する化合物を含む原料組成物と、水素および一酸化炭素とを反応させることを含むヒドロホルミル化方法が提供され、このヒドロホルミル化方法は、少なくとも2つの反応領域において実施され、この少なくとも2つの反応領域は、初期反応領域および後期反応領域を含み、後期反応領域の温度は、初期反応領域の温度よりも少なくとも2℃高く、後期反応領域の温度は、140℃から220℃の範囲内であり、初期反応領域の温度は、少なくとも130℃である。
本発明のヒドロホルミル化方法は、少なくとも2つの反応領域において実施される。
9−ヒドロカルビル−9−ホスファビシクロ[4.2.1]ノナン;
9−アリール−9−ホスファビシクロ[4.2.1]ノナン、
9−フェニル−9−ホスファビシクロ[4.2.1]ノナンなど;
(ジ)アルキル−9−アリール−9−ホスファビシクロ[4.2.1]ノナン、
3,7−ジメチル−9−フェニル−9−ホスファビシクロ[4.2.1]−ノナンなど、および
3,8−ジメチル−9−フェニル−9−ホスファビシクロ[4.2.1]ノナン;
9−アルキル−9−ホスファビシクロ[4.2.1]ノナン、
9−オクタデシル−9−ホスファビシクロ[4.2.1]ノナンなど、
9−ヘキシル−9−ホスファビシクロ[4.2.1]ノナン、
9−エイコシル−9−ホスファビシクロ[4.2.1]ノナン、および
9−トリアコンチル−9−ホスファビシクロ[4.2.1]ノナン;
9−シクロアルキル−9−ホスファビシクロ[4.2.1]ノナン、
9−シクロヘキシル−9−ホスファビシクロ[4.2.1]ノナンなど、および
9−(1−オクタヒドロペンタリル)−9−ホスファビシクロ[4.2.1]ノナン;
9−シクロアルケニル−9−ホスファビシクロ[4.2.1]ノナン、
9−シクロオクテニル−9−ホスファビシクロ[4.2.1]ノナンなど;
9−ヒドロカルビル−9−ホスファビシクロ[3.3.1]ノナン;
9−アリール−9−ホスファビシクロ[3.3.1]ノナン、
9−フェニル−9−ホスファビシクロ[3.3.1]ノナンなど;
9−アルキル−9−ホスファビシクロ[3.3.1]ノナン、
9−ヘキシル−9−ホスファビシクロ[3.3.1]ノナンなど、および
9−エイコシル−9−ホスファビシクロ[3.3.1]ノナン、ならびにこれらの混合物。
CH3(CH2)3CH=CH2+CO+H2→CH3(CH2)5CHOおよび/またはCH3(CH2)5CH2OH+異性体生成物
CH2=CHCl+CO+H2→ClCH2CH2CH2OHおよび/またはClCH2CH2CHO
CH3COOCH2CH=CH2+CO+H2→CH3COOCH2CH2CH2CHOおよび/またはCH3COOCH2CH2CH2CH2OH
シクロペンテン+CO+H2→ホルミルシクロペンタンおよび/またはシクロペンチルカルビノール
C2H5OCOCH=CHCOOC2H5+CO+H2→C2H5OCOCH(CHO)CH2COOC2H5および/またはC2H5OCOC(CH2OH)HCH2COOC2H5
アリルベンゼン+CO+H2→γ−フェニルブチルアルデヒドおよび/またはδ−フェニルブタノール+異性体生成物
Shell製のNEODENE−1112オレフィンのオレフィン原料組成物(これは、直鎖C11オレフィンおよびC12オレフィンの混合物を含む。)を上述の一連の反応器においてヒドロホルミル化した。一連の反応器中のコバルトの濃度を、反応器の全含量に基づいて0.28重量%の標的濃度に維持した。反応器の温度は、192℃であった。
Shell製のNEODENE−1112オレフィンのオレフィン原料組成物(これは、直鎖C11オレフィンおよびC12オレフィンの混合物を含む。)を上述の一連の反応器においてヒドロホルミル化した。一連の反応器中のコバルト濃度を、反応器の全含量に基づいて0.30重量%の標的濃度に維持した。
Shell製のNEODENE−1314オレフィンのオレフィン原料組成物(これは、直鎖C13オレフィンおよびC14オレフィンの混合物を含む。)を上述の一連の反応器においてヒドロホルミル化した。一連の反応器中のコバルトの濃度を、反応器の全含量に基づいて0.30重量%の標的濃度に維持した。
Shell製のNEODENE−1314オレフィンのオレフィン原料組成物(これは、直鎖C13オレフィンおよびC14オレフィンの混合物を含む。)を上述の一連の反応器においてヒドロホルミル化した。一連の反応器中のコバルトの濃度を、反応器の全含量に基づいて0.32重量%の標的濃度に維持した。
Claims (10)
- 有機ホスフィン修飾されたコバルトヒドロホルミル化触媒の存在下、少なくとも1つのオレフィン性炭素−炭素結合を有する化合物を含む原料組成物と、水素および一酸化炭素とを反応させることを含むヒドロホルミル化方法であり、前記ヒドロホルミル化方法が、少なくとも2つの反応領域において実施され、この少なくとも2つの反応領域が、初期反応領域および後期反応領域を含み、後期反応領域の温度が、初期反応領域における温度よりも少なくとも2℃高く、後期反応領域の温度が、140℃から220℃の範囲内であり、初期反応領域の温度が、少なくとも130℃である、前記ヒドロホルミル化方法。
- 後期反応領域の温度が、145℃から215℃の範囲内である、請求項1の方法。
- 後期反応領域の温度が、150℃から210℃の範囲内である、請求項1または請求項2の方法。
- 初期反応領域の温度が、少なくとも135℃である、請求項1から請求項3のいずれか一項の方法。
- 初期反応領域の温度が、少なくとも140℃である、請求項1から請求項4のいずれか一項の方法。
- 有機ホスフィン修飾されたコバルトヒドロホルミル化触媒が、一酸化炭素および有機ホスフィン配位子との錯体化合物におけるコバルトを含み、前記有機ホスフィン配位子が、1個の利用可能な電子対または非共有電子対を有する3価リン原子を有する、請求項1から請求項5のいずれか一項の方法。
- 有機ホスフィン配位子が、二環式のヘテロ環のtert−ホスフィン配位子である、請求項1から請求項6のいずれか一項の方法。
- 水素と一酸化炭素との比率が、1:1から10:1の範囲内である、請求項1から請求項7のいずれか一項の方法。
- 少なくとも1つのオレフィン性炭素−炭素結合を有する化合物が、少なくとも1つのオレフィン性炭素−炭素結合を有する直鎖化合物である、請求項1から請求項8のいずれか一項の方法。
- 原料組成物が、6から18個の炭素原子を有するオレフィン化合物を含む、請求項1から請求項9のいずれか一項の方法。
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EP05254142 | 2005-06-30 | ||
PCT/EP2006/063719 WO2007003589A1 (en) | 2005-06-30 | 2006-06-30 | Hydroformylation process |
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EP (1) | EP1899290B1 (ja) |
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CN (1) | CN101228106B (ja) |
AT (1) | ATE495142T1 (ja) |
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GB2458051B (en) * | 2006-12-21 | 2011-06-29 | Shell Int Research | Hydroformylation process |
GB2461827B (en) * | 2007-05-23 | 2011-12-07 | Shell Int Research | Hydroformylation process |
GB2461479B (en) * | 2007-05-23 | 2011-08-24 | Shell Int Research | Hydroformylation process |
US7767862B2 (en) | 2008-08-11 | 2010-08-03 | Shell Oil Company | Ligand, catalyst and process for hydroformylation |
CN102272083B (zh) * | 2009-01-08 | 2015-01-21 | 埃克森美孚化学专利公司 | 醇或者与醇有关的改进 |
WO2012072594A1 (en) | 2010-11-30 | 2012-06-07 | Shell Internationale Research Maatschappij B.V. | Ligand, catalyst and process for hydroformylation |
CA2823149A1 (en) | 2010-12-29 | 2012-07-05 | Shell Internationale Research Maatschappij B.V. | Method and composition for enhanced hydrocarbons recovery from a formation containing a crude oil |
WO2013181083A1 (en) | 2012-05-29 | 2013-12-05 | Shell Oil Company | A laundry detergent composition and method of making thereof |
WO2015018710A1 (de) * | 2013-08-08 | 2015-02-12 | Basf Se | Verfahren zum entfernen von cobaltablagerungen in einem olefin hochdruckhydroformylierung reaktor |
BR112016013001B1 (pt) | 2013-12-19 | 2020-12-29 | Dow Technology Investments Llc | processo de hidroformilação |
KR102310130B1 (ko) * | 2014-09-01 | 2021-10-08 | 삼성전자주식회사 | 착용 가능한 전자 장치 |
CN110981692A (zh) * | 2019-12-25 | 2020-04-10 | 中国科学院兰州化学物理研究所 | 一种联产异壬醇和碳八烷烃的方法及系统 |
CN115701418B (zh) * | 2021-08-02 | 2024-05-17 | 中国石油化工股份有限公司 | 醛醇组合物及其制备方法、一种连续制备醛、醇的方法 |
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US3369050A (en) | 1961-10-06 | 1968-02-13 | Shell Oil Co | Separation, recovery and recycle of the catalyst complex in the oxo process |
US3501515A (en) | 1965-03-29 | 1970-03-17 | Shell Oil Co | Bicyclic heterocyclic tertiary phosphine-cobalt-carbonyl complexes |
US3420898A (en) | 1965-03-29 | 1969-01-07 | Shell Oil Co | Single stage hydroformylation of olefins to alcohols |
US3448157A (en) | 1965-09-27 | 1969-06-03 | Shell Oil Co | Hydroformylation of olefins |
US3448158A (en) | 1966-01-28 | 1969-06-03 | Shell Oil Co | Hydroformylation of olefins |
US3904547A (en) | 1973-06-06 | 1975-09-09 | Gen Electric | Process for recycling a cobalt hydroformylation catalyst |
US5112519A (en) * | 1989-06-05 | 1992-05-12 | Mobil Oil Corporation | Process for production of biodegradable surfactants and compositions thereof |
US5741944A (en) * | 1995-12-06 | 1998-04-21 | Union Carbide Chemicals & Plastics Technology Corporation | Hydroformaylation processes |
DE19617257A1 (de) * | 1996-04-30 | 1997-11-06 | Hoechst Ag | Verfahren zur Hydroformylierung olefinisch ungesättigter Verbindungen |
KR20020033785A (ko) | 1999-09-06 | 2002-05-07 | 사또, 후미에 | 프로스타글란딘 e 유사체 |
DE10034360A1 (de) | 2000-07-14 | 2002-01-24 | Oxeno Olefinchemie Gmbh | Mehrstufiges Verfahren zur Herstellung von Oxo-Aldehyden und/oder Alkoholen |
ATE401292T1 (de) | 2003-10-21 | 2008-08-15 | Basf Se | Verfahren zur kontinuierlichen herstellung von aldehyden |
DE10357718A1 (de) | 2003-12-09 | 2005-07-21 | Basf Ag | Verfahren zur Herstellung von Tricyclodecandialdehyd |
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EP1899290A1 (en) | 2008-03-19 |
ZA200711026B (en) | 2008-11-26 |
CN101228106B (zh) | 2011-09-14 |
US7329783B2 (en) | 2008-02-12 |
WO2007003589A1 (en) | 2007-01-11 |
JP2008544971A (ja) | 2008-12-11 |
CA2612596C (en) | 2013-11-26 |
CN101228106A (zh) | 2008-07-23 |
ATE495142T1 (de) | 2011-01-15 |
US20070015942A1 (en) | 2007-01-18 |
DE602006019592D1 (en) | 2011-02-24 |
EP1899290B1 (en) | 2011-01-12 |
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