JP2012140332A - オレフィンの製造法 - Google Patents
オレフィンの製造法 Download PDFInfo
- Publication number
- JP2012140332A JP2012140332A JP2010291848A JP2010291848A JP2012140332A JP 2012140332 A JP2012140332 A JP 2012140332A JP 2010291848 A JP2010291848 A JP 2010291848A JP 2010291848 A JP2010291848 A JP 2010291848A JP 2012140332 A JP2012140332 A JP 2012140332A
- Authority
- JP
- Japan
- Prior art keywords
- group
- acid
- metals
- olefin
- hydrogen atom
- 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.)
- Granted
Links
- 150000001336 alkenes Chemical class 0.000 title claims abstract description 44
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 title claims abstract description 41
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 17
- 229910052751 metal Inorganic materials 0.000 claims abstract description 82
- 239000002184 metal Substances 0.000 claims abstract description 64
- 150000002739 metals Chemical class 0.000 claims abstract description 53
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 38
- 229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 38
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract description 33
- 239000003054 catalyst Substances 0.000 claims abstract description 32
- 238000006606 decarbonylation reaction Methods 0.000 claims abstract description 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 41
- 238000006243 chemical reaction Methods 0.000 claims description 37
- 239000007789 gas Substances 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 23
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 12
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 7
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 6
- 229910052740 iodine Inorganic materials 0.000 claims description 6
- 239000011630 iodine Substances 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 4
- 125000003368 amide group Chemical group 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 229910052800 carbon group element Inorganic materials 0.000 claims description 2
- 125000004185 ester group Chemical group 0.000 claims description 2
- 125000001033 ether group Chemical group 0.000 claims description 2
- 229910052727 yttrium Inorganic materials 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 30
- 239000003446 ligand Substances 0.000 description 24
- 239000012071 phase Substances 0.000 description 17
- 150000008065 acid anhydrides Chemical class 0.000 description 14
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Substances [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 14
- 239000002253 acid Substances 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 12
- 235000021355 Stearic acid Nutrition 0.000 description 11
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 11
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 11
- 239000008117 stearic acid Substances 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- KHAVLLBUVKBTBG-UHFFFAOYSA-N dec-9-enoic acid Chemical compound OC(=O)CCCCCCCC=C KHAVLLBUVKBTBG-UHFFFAOYSA-N 0.000 description 10
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 9
- WSWCOQWTEOXDQX-UHFFFAOYSA-N 2,4-Hexadienoic acid Chemical compound CC=CC=CC(O)=O WSWCOQWTEOXDQX-UHFFFAOYSA-N 0.000 description 8
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 8
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 8
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 8
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 8
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 8
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 8
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 8
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 8
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 8
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 8
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 8
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 8
- 239000010949 copper Substances 0.000 description 7
- 239000002994 raw material Substances 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 6
- -1 carboxylic acid halide Chemical class 0.000 description 6
- 229910052802 copper Inorganic materials 0.000 description 6
- 229910052741 iridium Inorganic materials 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 229910052696 pnictogen Inorganic materials 0.000 description 6
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 5
- LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 5
- 235000002597 Solanum melongena Nutrition 0.000 description 5
- 229910052759 nickel Inorganic materials 0.000 description 5
- 229910052703 rhodium Inorganic materials 0.000 description 5
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 5
- 229960003656 ricinoleic acid Drugs 0.000 description 5
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 4
- QFMZQPDHXULLKC-UHFFFAOYSA-N 1,2-bis(diphenylphosphino)ethane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)CCP(C=1C=CC=CC=1)C1=CC=CC=C1 QFMZQPDHXULLKC-UHFFFAOYSA-N 0.000 description 4
- YIWGJFPJRAEKMK-UHFFFAOYSA-N 1-(2H-benzotriazol-5-yl)-3-methyl-8-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carbonyl]-1,3,8-triazaspiro[4.5]decane-2,4-dione Chemical compound CN1C(=O)N(c2ccc3n[nH]nc3c2)C2(CCN(CC2)C(=O)c2cnc(NCc3cccc(OC(F)(F)F)c3)nc2)C1=O YIWGJFPJRAEKMK-UHFFFAOYSA-N 0.000 description 4
- FRPZMMHWLSIFAZ-UHFFFAOYSA-N 10-undecenoic acid Chemical compound OC(=O)CCCCCCCCC=C FRPZMMHWLSIFAZ-UHFFFAOYSA-N 0.000 description 4
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 4
- GWYFCOCPABKNJV-UHFFFAOYSA-M 3-Methylbutanoic acid Natural products CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 description 4
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 4
- 235000021357 Behenic acid Nutrition 0.000 description 4
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 4
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 4
- 239000005639 Lauric acid Substances 0.000 description 4
- 101100030361 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) pph-3 gene Proteins 0.000 description 4
- 239000005642 Oleic acid Substances 0.000 description 4
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 4
- 235000021314 Palmitic acid Nutrition 0.000 description 4
- 239000001361 adipic acid Substances 0.000 description 4
- 235000011037 adipic acid Nutrition 0.000 description 4
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 4
- 229940116226 behenic acid Drugs 0.000 description 4
- LVTCZSBUROAWTE-UHFFFAOYSA-N diethyl(phenyl)phosphane Chemical compound CCP(CC)C1=CC=CC=C1 LVTCZSBUROAWTE-UHFFFAOYSA-N 0.000 description 4
- HASCQPSFPAKVEK-UHFFFAOYSA-N dimethyl(phenyl)phosphine Chemical compound CP(C)C1=CC=CC=C1 HASCQPSFPAKVEK-UHFFFAOYSA-N 0.000 description 4
- WUOIAOOSKMHJOV-UHFFFAOYSA-N ethyl(diphenyl)phosphane Chemical compound C=1C=CC=CC=1P(CC)C1=CC=CC=C1 WUOIAOOSKMHJOV-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 4
- UJNZOIKQAUQOCN-UHFFFAOYSA-N methyl(diphenyl)phosphane Chemical compound C=1C=CC=CC=1P(C)C1=CC=CC=C1 UJNZOIKQAUQOCN-UHFFFAOYSA-N 0.000 description 4
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 4
- WVJVHUWVQNLPCR-UHFFFAOYSA-N octadecanoyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(=O)CCCCCCCCCCCCCCCCC WVJVHUWVQNLPCR-UHFFFAOYSA-N 0.000 description 4
- 229960002446 octanoic acid Drugs 0.000 description 4
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
- 229910052763 palladium Inorganic materials 0.000 description 4
- 229910052697 platinum Inorganic materials 0.000 description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 4
- 235000010199 sorbic acid Nutrition 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 4
- BWHDROKFUHTORW-UHFFFAOYSA-N tritert-butylphosphane Chemical compound CC(C)(C)P(C(C)(C)C)C(C)(C)C BWHDROKFUHTORW-UHFFFAOYSA-N 0.000 description 4
- 229960002703 undecylenic acid Drugs 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 3
- 101150003085 Pdcl gene Proteins 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 230000002194 synthesizing effect Effects 0.000 description 3
- 239000004711 α-olefin Substances 0.000 description 3
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 description 2
- 239000004912 1,5-cyclooctadiene Substances 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- PGZVFRAEAAXREB-UHFFFAOYSA-N 2,2-dimethylpropanoyl 2,2-dimethylpropanoate Chemical compound CC(C)(C)C(=O)OC(=O)C(C)(C)C PGZVFRAEAAXREB-UHFFFAOYSA-N 0.000 description 2
- ADLVDYMTBOSDFE-UHFFFAOYSA-N 5-chloro-6-nitroisoindole-1,3-dione Chemical compound C1=C(Cl)C([N+](=O)[O-])=CC2=C1C(=O)NC2=O ADLVDYMTBOSDFE-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- 101100189618 Caenorhabditis elegans pdi-2 gene Proteins 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 229910052785 arsenic Inorganic materials 0.000 description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 125000003262 carboxylic acid ester group Chemical class [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- ZXKWUYWWVSKKQZ-UHFFFAOYSA-N cyclohexyl(diphenyl)phosphane Chemical compound C1CCCCC1P(C=1C=CC=CC=1)C1=CC=CC=C1 ZXKWUYWWVSKKQZ-UHFFFAOYSA-N 0.000 description 2
- 238000005262 decarbonization Methods 0.000 description 2
- YNHIGQDRGKUECZ-UHFFFAOYSA-N dichloropalladium;triphenylphosphanium Chemical compound Cl[Pd]Cl.C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 229910001849 group 12 element Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- IFXORIIYQORRMJ-UHFFFAOYSA-N tribenzylphosphane Chemical compound C=1C=CC=CC=1CP(CC=1C=CC=CC=1)CC1=CC=CC=C1 IFXORIIYQORRMJ-UHFFFAOYSA-N 0.000 description 2
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 2
- WLPUWLXVBWGYMZ-UHFFFAOYSA-N tricyclohexylphosphine Chemical compound C1CCCCC1P(C1CCCCC1)C1CCCCC1 WLPUWLXVBWGYMZ-UHFFFAOYSA-N 0.000 description 2
- IGNTWNVBGLNYDV-UHFFFAOYSA-N triisopropylphosphine Chemical compound CC(C)P(C(C)C)C(C)C IGNTWNVBGLNYDV-UHFFFAOYSA-N 0.000 description 2
- UYUUAUOYLFIRJG-UHFFFAOYSA-N tris(4-methoxyphenyl)phosphane Chemical compound C1=CC(OC)=CC=C1P(C=1C=CC(OC)=CC=1)C1=CC=C(OC)C=C1 UYUUAUOYLFIRJG-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- NGEZPLCPKXKLQQ-VOTSOKGWSA-N (e)-4-(3-methoxyphenyl)but-3-en-2-one Chemical compound COC1=CC=CC(\C=C\C(C)=O)=C1 NGEZPLCPKXKLQQ-VOTSOKGWSA-N 0.000 description 1
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- JPSKCQCQZUGWNM-UHFFFAOYSA-N 2,7-Oxepanedione Chemical compound O=C1CCCCC(=O)O1 JPSKCQCQZUGWNM-UHFFFAOYSA-N 0.000 description 1
- FREZLSIGWNCSOQ-UHFFFAOYSA-N 3-methylbutanoyl 3-methylbutanoate Chemical compound CC(C)CC(=O)OC(=O)CC(C)C FREZLSIGWNCSOQ-UHFFFAOYSA-N 0.000 description 1
- SQAHPYZABTWPNY-UHFFFAOYSA-N 3-phenylpropanoyl 3-phenylpropanoate Chemical compound C=1C=CC=CC=1CCC(=O)OC(=O)CCC1=CC=CC=C1 SQAHPYZABTWPNY-UHFFFAOYSA-N 0.000 description 1
- UITKHKNFVCYWNG-UHFFFAOYSA-N 4-(3,4-dicarboxybenzoyl)phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1C(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 UITKHKNFVCYWNG-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- XADKGDBMULSEAC-UHFFFAOYSA-N Gorlic acid Natural products OC(=O)CCCCC=CCCCCCCC1CCC=C1 XADKGDBMULSEAC-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 1
- OCNZHGHKKQOQCZ-CLFAGFIQSA-N [(z)-octadec-9-enoyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC(=O)CCCCCCC\C=C/CCCCCCCC OCNZHGHKKQOQCZ-CLFAGFIQSA-N 0.000 description 1
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- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical compound O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- RCRYHUPTBJZEQS-UHFFFAOYSA-N tetradecanoyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OC(=O)CCCCCCCCCCCCC RCRYHUPTBJZEQS-UHFFFAOYSA-N 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- XGOZKNCGVJSRKD-UHFFFAOYSA-N undec-10-enoyl undec-10-enoate Chemical compound C=CCCCCCCCCC(=O)OC(=O)CCCCCCCCC=C XGOZKNCGVJSRKD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/20—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms
- C07C1/207—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms from carbonyl compounds
- C07C1/2078—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms from carbonyl compounds by a transformation in which at least one -C(=O)-O- moiety is eliminated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/02—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the alkali- or alkaline earth metals or beryllium
- C07C2523/04—Alkali metals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- C07C2531/20—Carbonyls
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- C07C2531/24—Phosphines
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups C07C2531/02 - C07C2531/24
- C07C2531/28—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups C07C2531/02 - C07C2531/24 of the platinum group metals, iron group metals or copper
- C07C2531/30—Halides
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
【解決手段】一酸化炭素濃度が41mmol/L以上の条件にて、第9族金属、第10族金属、第11族金属からなる群から選ばれる一種以上の金属元素を含む触媒の存在下、β水素原子を有するカルボン酸又はその誘導体の脱カルボニル反応を行う、オレフィンの製造法。
【選択図】なし
Description
態様1において用いる触媒は、第9族金属、第10族金属、第11族金属からなる群から選ばれる一種以上の金属元素を含む触媒である。反応性、選択性の観点から、第9族金属、第10族金属、第11族金属からなる群から選ばれる一種以上の金属元素としては、Co、Rh、Ir、Ni、Pd、Pt、Cuが好ましく、Co、Rh、Ir、Ni、Pd、Cuがより好ましく、Niが更に好ましい。第9族金属、第10族金属、第11族金属からなる群から選ばれる一種以上の金属元素を含む触媒としては、具体的には、[RhCl(CO)2]2、(Ph3P)2Rh(CO)Cl、RhCl3、(Ph3P)2NiCl2、NiCl2、(Ph3P)2PdCl2、PdCl2、(Ph3P)2CoCl2、CoCl2、(Ph3P)2PtCl2、PtCl2、(Ph3P)2Ir(CO)Cl、Ir(CO)3Cl、IrCl3、(Ph3P)3CuCl、CuCl(式中、Phはフェニル基を示す、以下同様)などが挙げられ、[RhCl(CO)2]2、(Ph3P)2PdCl2、(Ph3P)2CoCl2、Ir(CO)3Cl、(Ph3P)2NiCl2、CuCl等が好ましく、特に(Ph3P)2NiCl2が好ましい。
(式中、Rは炭素数1〜22の炭化水素基を示し、Yは−Z−(CH2)m−で示される基を示し、Zはエーテル基、アミノ基、アミド基又はエステル基、より具体的には−O−、−NH−、−CONH−、−NHCO−、−COO−又は−OCO−、mは1〜6の数を示し、nは0又は1を示し、複数個のR、Y及びnはそれぞれ同一でも異なっていても良い。また、[R−(Y)n]同士の間で環状構造を形成していてもよい。)
この方法では、生成する水や目的物を系外に留出させつつ、反応させることもできる。
本発明の態様2において用いる触媒は、第9族金属、第10族金属、第11族金属からなる群から選ばれる一種以上の金属元素とヨウ素元素を含む化合物である。反応性、選択性の観点から、第9族金属、第10族金属、第11族金属からなる群から選ばれる一種以上の金属元素としては、Co、Rh、Ir、Ni、Pd、Pt、Cu、Ag、Auが挙げられ、Co、Rh、Ir、Ni、Ptが好ましく、Niがより好ましい。第9族金属、第10族金属、第11族金属からなる群から選ばれる一種以上の金属元素とヨウ素元素を含む化合物の具体例としては、CoI2、CoI2(CO)(C5H5)、CoI2(PPh3)(C5H5)、CoI2(PPh3)2、RhI3、[RhI(CO)2]2、RhI(PPh3)3、IrI4、IrI(CO)(PPh3)2、NiI2、NiI2(NH3)6、NiI(1,5−シクロオクタジエン)、NiI(PPh3)3、PdI2、PdI2(PPh3)2、PdI(CH3)(PPh3)2、PtI2、[Pt2I2(H2NCH2CH2NH2)2](NO3)2、PtI2(1,5−シクロオクタジエン)、PtI(CH3)3、PtI(CH3)(PEt3)2、CuI、AgI、AuI、AuI(CH3)2(PPh3)(式中、Phはフェニル基、Etはエチル基を示す、以下同様)などが挙げられ、CoI2、RhI3、[RhI(CO)2]2、IrI(CO)(PPh3)2、NiI2、PtI2が好ましく、NiI2がより好ましい。
30mLステンレス製オートクレーブに、撹拌子と、ステアリン酸 284.5mg(1.0mmol)、NiCl2(PPh3)2 6.5mg(0.01mmol)、トリフェニルホスフィン(PPh3) 5.2mg(0.02mmol)、ヨウ化カリウム 16.6mg(0.1mmol)を加え、室温(25℃)にて容器内に一酸化炭素を3000kPa(絶対圧)導入、常圧に戻す置換操作を3回行った。その後、室温にて一酸化炭素608kPa(絶対圧)を導入後、系を密閉し、攪拌を開始した後、昇温し250℃で3時間攪拌した。気相中の一酸化炭素濃度は246mmol/Lである。その後、加熱をやめ、室温(25℃)になるまで放置した。低沸分を減圧留去したのち、内部標準としてアニソールを加え、1H−NMR測定より、生成物を定量した(生成物の定量は、ステアリン酸のα位のプロトン、末端オレフィンのビニルプロトン、内部オレフィンのビニルプロトン、内部標準であるアニソールのメチル基との積分比を比較することにより行った)。
仕込みステアリン酸に対してオレフィンが収率31%(末端オレフィン:内部オレフィン(モル比)=42:58)で得られた。
触媒の種類及び量、トリフェニルホスフィンの量を表1に示すものへと変えた以外は実施例1−1と同様に行った。
触媒の種類及び量、トリフェニルホスフィンの量を表1に示すものへと変え、20mLナスフラスコを用い、減圧−リークによる窒素置換を3回行った後、真空ポンプをつなぎ、33kPa(絶対圧)下で反応を行った以外は実施例1−1と同様にいった。このときの気相中の一酸化炭素濃度は、0mmol/L(反応初期)〜3.8(反応終期最大値)mmol/Lであった。
なお、気相中の一酸化炭素濃度の反応終期最大値は下記のように見積もったものである。
すなわち、反応によって、水及びCOが0.1molずつ発生する。減圧下250℃という高温なので水は全て気化すると考えられるから、33kPaの半分がCOと考えられる。従って、気相中の一酸化炭素濃度の最大値は以下の通り見積もられる。
33/2/101.3 ÷ 22.4 × 273.15/(273.15+250) × 1000 = 3.8mmol/L
反応圧力を表2に示すものへと変えた以外は実施例1−1と同様に行った。
原料のステアリン酸を無水ステアリン酸に変え、200℃で反応を行った以外は実施例1−1と同様に行った。
触媒の種類及び量、トリフェニルホスフィンの量を表3に示すものへと変え、20mLナスフラスコを用い、窒素置換を3回行った後、真空ポンプをつなぎ、33kPa(絶対圧)下で反応を行った以外は実施例1−9と同様に行った。
30mLステンレス製オートクレーブに、撹拌子と、ステアリン酸 284.5mg(1.0mmol)、NiI2 3.1mg(0.01mmol)、トリフェニルホスフィン(PPh3) 10.4mg(0.04mmol)を加え、室温(25℃)にて容器内に一酸化炭素を3000kPa(絶対圧)導入、常圧に戻す置換操作を3回行った。その後、室温にて一酸化炭素608kPa(絶対圧)を導入後、系を密閉し、攪拌を開始した後、昇温し250℃で3時間攪拌した。その後、加熱をやめ、室温(25℃)になるまで放置した。低沸分を減圧留去したのち、実施例1−1と同様に1H−NMR測定より、生成物を定量した。
仕込みステアリン酸に対してオレフィンが収率21%(末端オレフィン:内部オレフィン(モル比)=42:58)で得られた。
20mLナスフラスコを用い、窒素置換を3回行った後、真空ポンプをつなぎ、33kPa(絶対圧)下で反応を行った以外は実施例2−1と同様に行った。
ヨウ化カリウムを添加しなかった以外は実施例1−1と同様に行った。
20mLナスフラスコを用い、窒素置換を3回行った後、真空ポンプをつなぎ、33kPa(絶対圧)下で反応を行った以外は実施例3−1と同様に行った。
ヨウ化カリウムを添加しなかった以外は実施例1−9と同様に行った。
触媒の種類、トリフェニルホスフィンの量を表6に示すものへと変え、20mLナスフラスコを用い、窒素置換を3回行った後、真空ポンプをつなぎ、33kPa(絶対圧)下で反応を行った以外は実施例3−2と同様に行った。
・ステアリン酸:Nacalai Tesque社製、品番 32202−25
・無水ステアリン酸:東京化成工業社製、品番 S0083
・NiCl2(PPh3)2:東京化成工業社製、品番 B1571
・[RhCl(CO)2]2:RhCl3・nH2O(田中貴金属販売(株))より調製
・IrCl(CO)3:ACROS社製、 品番 36355-1000
・PdCl2(PPh3)2:PdCl2(和光純薬工業社製、品番162−00053)より調製
・CuCl:Nacalai Tesque社製、品番 09508−42
・NiI2:Aldrich社製、品番 400777−5G
・NiCl2:石津製薬社製、品番 043−2761
・トリフェニルホスフィン:Nacalai Tesque社製、品番 35312−82
・ヨウ化カリウム:和光純薬工業社製、品番 162−19642
Claims (5)
- 第9族金属、第10族金属、第11族金属からなる群から選ばれる一種以上の金属元素を含む触媒の存在下、β水素原子を有するカルボン酸又はその誘導体の脱カルボニル反応を行う、オレフィンの製造法であって、反応時の気相中の一酸化炭素濃度を41mmol/L以上の条件にて行う、オレフィンの製造方法。
- 第9族金属、第10族金属、第11族金属からなる群から選ばれる一種以上の金属元素を含む触媒とヨウ化物の存在下に脱カルボニル化反応を行う、請求項1記載のオレフィンの製造法。
- ヨウ化物が、第1族元素〜第8族元素及び第12族元素〜第14族元素から選ばれる元素のヨウ化物、又は下記一般式(1)で示される4級アンモニウム化合物である、請求項2記載のオレフィンの製造法。
[R−(Y)n]4N+I− (1)
(ここで、Rは炭素数1〜22の炭化水素基を示し、Yは−Z−(CH2)m−で示される基を示し、Zはエーテル基、アミノ基、アミド基又はエステル基、mは1〜6の数を示し、nは0又は1を示し、複数個のR、Y及びnはそれぞれ同一でも異なっていても良い。また、[R−(Y)n]同士の間で環状構造を形成していてもよい。) - 第9族金属、第10族金属、第11族金属からなる群から選ばれる一種以上の金属元素とヨウ素元素を含む化合物を触媒として用いて脱カルボニル化反応を行う、請求項1記載のオレフィンの製造法。
- β水素原子を有するカルボン酸又はその誘導体が、β水素原子を有するカルボン酸又はβ水素原子を有するカルボン酸無水物である、請求項1〜4の何れか1項記載のオレフィンの製造法。
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US13/976,706 US9266790B2 (en) | 2010-12-28 | 2011-08-04 | Method for producing olefin |
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MYPI2013701117A MY171725A (en) | 2010-12-28 | 2011-08-04 | Method for producing olefin |
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JP2014213225A (ja) * | 2013-04-23 | 2014-11-17 | 花王株式会社 | Pd化合物担持触媒 |
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WO2024038044A1 (en) * | 2022-08-17 | 2024-02-22 | Basf Se | Process for the preparation of bio-based olefins from primary alcohol |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5077447A (en) * | 1990-09-28 | 1991-12-31 | Henkel Research Corporation | Process for making olefins |
WO2010024420A1 (ja) * | 2008-08-25 | 2010-03-04 | 花王株式会社 | オレフィンの製造法 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3530198A (en) | 1968-04-02 | 1970-09-22 | Union Oil Co | Process for preparation of olefins |
JPH10168340A (ja) | 1996-12-13 | 1998-06-23 | Tokio Saitou | 無機質系水性塗装材 |
JP5554968B2 (ja) | 2009-11-12 | 2014-07-23 | 花王株式会社 | オレフィンの製造法 |
JP2011168528A (ja) | 2010-02-18 | 2011-09-01 | Kao Corp | オレフィンの製造法 |
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- 2011-08-04 WO PCT/JP2011/067825 patent/WO2012090544A1/ja active Application Filing
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5077447A (en) * | 1990-09-28 | 1991-12-31 | Henkel Research Corporation | Process for making olefins |
WO2010024420A1 (ja) * | 2008-08-25 | 2010-03-04 | 花王株式会社 | オレフィンの製造法 |
Non-Patent Citations (3)
Title |
---|
JPN6010069789; GOOSSEN,L.J. et al: 'A mild and efficient protocol for the conversion of carboxylic acids to olefins by a catalytic decar' Chemical Communications No.6, 2004, p.724-725 * |
JPN6014044775; 日本化学会講演予稿集 Vol.90th, No.4, p.1202 (2010). * |
JPN6014044777; 日本化学会講演予稿集 Vol.89th, No.2, p.990 (2009). * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014175039A1 (ja) * | 2013-04-23 | 2014-10-30 | 花王株式会社 | オレフィンの製造方法 |
JP2014213225A (ja) * | 2013-04-23 | 2014-11-17 | 花王株式会社 | Pd化合物担持触媒 |
JP2014224098A (ja) * | 2013-04-23 | 2014-12-04 | 花王株式会社 | オレフィンの製造方法 |
CN105121392A (zh) * | 2013-04-23 | 2015-12-02 | 花王株式会社 | 烯烃的制造方法 |
CN105121392B (zh) * | 2013-04-23 | 2017-06-13 | 花王株式会社 | 烯烃的制造方法 |
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WO2012090544A1 (ja) | 2012-07-05 |
EP2660226A1 (en) | 2013-11-06 |
US20130296626A1 (en) | 2013-11-07 |
CN103282329B (zh) | 2016-03-23 |
JP5718634B2 (ja) | 2015-05-13 |
BR112013012764A2 (pt) | 2016-09-13 |
EP2660226B1 (en) | 2015-12-09 |
MY171725A (en) | 2019-10-25 |
US9266790B2 (en) | 2016-02-23 |
EP2660226A4 (en) | 2014-07-23 |
CN103282329A (zh) | 2013-09-04 |
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