DE1643063C - - Google Patents
Info
- Publication number
- DE1643063C DE1643063C DE1643063C DE 1643063 C DE1643063 C DE 1643063C DE 1643063 C DE1643063 C DE 1643063C
- Authority
- DE
- Germany
- Prior art keywords
- metal
- diolefins
- catalyst
- nickel
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 44
- 239000003054 catalyst Substances 0.000 claims description 28
- 238000006243 chemical reaction Methods 0.000 claims description 22
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 20
- 239000000047 product Substances 0.000 claims description 10
- RRKODOZNUZCUBN-CCAGOZQPSA-N (1z,3z)-cycloocta-1,3-diene Chemical compound C1CC\C=C/C=C\C1 RRKODOZNUZCUBN-CCAGOZQPSA-N 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 229910052759 nickel Inorganic materials 0.000 claims description 8
- ZCINTQHDIUHMKK-UHFFFAOYSA-N 1,1-bis(ethenyl)cyclobutane Chemical compound C=CC1(C=C)CCC1 ZCINTQHDIUHMKK-UHFFFAOYSA-N 0.000 claims description 6
- 150000001993 dienes Chemical class 0.000 claims description 6
- 239000007795 chemical reaction product Substances 0.000 claims description 5
- 230000003197 catalytic effect Effects 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical group C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 claims description 3
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 claims description 3
- 239000011541 reaction mixture Substances 0.000 claims description 3
- 230000002829 reductive effect Effects 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 238000010626 work up procedure Methods 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims 8
- 239000002184 metal Substances 0.000 claims 8
- 150000001875 compounds Chemical class 0.000 claims 6
- 238000004519 manufacturing process Methods 0.000 claims 6
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 238000006471 dimerization reaction Methods 0.000 claims 3
- 229910052987 metal hydride Inorganic materials 0.000 claims 3
- 150000004681 metal hydrides Chemical class 0.000 claims 3
- 150000002816 nickel compounds Chemical class 0.000 claims 3
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- 230000001603 reducing effect Effects 0.000 claims 2
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims 2
- MZJCFRKLOXHQIL-CCAGOZQPSA-N (1Z,3Z)-cyclodeca-1,3-diene Chemical compound C1CCC\C=C/C=C\CC1 MZJCFRKLOXHQIL-CCAGOZQPSA-N 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- 238000005684 Liebig rearrangement reaction Methods 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims 1
- 150000001728 carbonyl compounds Chemical class 0.000 claims 1
- 150000002009 diols Chemical class 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 150000008282 halocarbons Chemical class 0.000 claims 1
- 150000004678 hydrides Chemical class 0.000 claims 1
- 239000012442 inert solvent Substances 0.000 claims 1
- 230000001678 irradiating effect Effects 0.000 claims 1
- 229910052753 mercury Inorganic materials 0.000 claims 1
- 238000006384 oligomerization reaction Methods 0.000 claims 1
- -1 organometallic compounds cyclobutane derivatives Chemical class 0.000 claims 1
- 125000002524 organometallic group Chemical group 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 150000003623 transition metal compounds Chemical class 0.000 claims 1
- 150000005671 trienes Chemical class 0.000 claims 1
- 238000005829 trimerization reaction Methods 0.000 claims 1
- BBDKZWKEPDTENS-UHFFFAOYSA-N 4-Vinylcyclohexene Chemical compound C=CC1CCC=CC1 BBDKZWKEPDTENS-UHFFFAOYSA-N 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- SHWZFQPXYGHRKT-FDGPNNRMSA-N (z)-4-hydroxypent-3-en-2-one;nickel Chemical compound [Ni].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O SHWZFQPXYGHRKT-FDGPNNRMSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 230000008707 rearrangement Effects 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical group C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- OFZYBEBWCZBCPM-UHFFFAOYSA-N 1,1-dimethylcyclobutane Chemical compound CC1(C)CCC1 OFZYBEBWCZBCPM-UHFFFAOYSA-N 0.000 description 1
- JWTIFYFTDZFHPW-UHFFFAOYSA-N 4-ethenyl-1,2-dimethylcyclohexene Chemical compound CC1=C(C)CC(C=C)CC1 JWTIFYFTDZFHPW-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- CQYBWJYIKCZXCN-UHFFFAOYSA-N diethylaluminum Chemical compound CC[Al]CC CQYBWJYIKCZXCN-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- WLPUWLXVBWGYMZ-UHFFFAOYSA-N tricyclohexylphosphine Chemical compound C1CCCCC1P(C1CCCCC1)C1CCCCC1 WLPUWLXVBWGYMZ-UHFFFAOYSA-N 0.000 description 1
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 1
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP1860086B1 (de) | Verfahren zur Herstellung von Cyclododecatrien | |
| DE2405856A1 (de) | Katalytische dimerisierung von konjugierten dienen und katalysator dafuer | |
| CH498061A (de) | Verfahren zur katalytischen Di- bzw. Trimerisation von 1,3-Diolefinen | |
| DE1126864B (de) | Verfahren zur Herstellung von cyclischen Dimeren neben anderen fluessigen Oligomeren on 1, 3-Dienen | |
| DE2350689C2 (de) | Verfahren zur Dimerisierung bzw. Codimerisierung von bestimmten Diolefinen und Katalysator für die Durchführung dieses Verfahrens | |
| DE1643063C (https=) | ||
| EP1843994B1 (de) | Verfahren zur herstellung von trimethylcyclododecatrien unter verwendung eines titan-katalysators | |
| DE1955933C3 (de) | Verfahren zur Herstellung von 1-Alkoxyoctadienen-(2,7) | |
| DE1643063B1 (de) | Verfahren zur Cyclodimerisation von 1,3-Diolefinen mittels Nickel enthaltender Katalysatoren | |
| DE1468271C3 (https=) | ||
| DE1239304B (de) | Verfahren zur Herstellung der Dimeren des Bicyclo-[2, 2, 1]-heptadiens-2, 5 und seiner unterhalb 140 siedenden Alkylderivate | |
| DE1810185B2 (de) | Nickel (0)-katalysatoren, Verfahren zu deren Herstellung und deren Verwendung zur Oligomerisation von Butadien | |
| DE1288087B (de) | Verfahren zur Mischoligomerisation unter Verwendung von 1,3-Diolefinen in Gegenwart eines kohlenoxydfreien Organo-Metallkoinplexkatalysators der Übergangsmetalle der VIII. Nebengruppe | |
| DD240198A1 (de) | Verfahren zur katalytischen cyclisierung von alkinen | |
| DE1643832C3 (de) | Verfahren zur Herstellung nickelhaltiger Cyclooligomerisierungskatalysatoren | |
| DE1493221A1 (de) | Substituierte 8-,10- und 12-Ringe und Verfahren zu ihrer Herstellung durch katalytische Co-Oligomerisation von ungesaettigten Verbindungen | |
| DE1593268C3 (de) | Verfahren zur Cyclodimerisation von 1,3-Butadien oder Isopren oder Mischungen davon mittels eines metallorganischen Mischkatalysators | |
| DE1593533C3 (de) | Verfahren zur Herstellung von Cyclododecatrien-(1,5,9) | |
| DE1443653C (de) | Verfahren zur Isomerisierung eines öle finischen Kohlenwasserstoffs über einem Ka talysator aus einem Eisensalz und einer aluminiumorganischen Verbindung | |
| DE1298525B (de) | Verfahren zur Herstellung von Cyclooktadien-(1, 5) aus Butadien in Gegenwart eines komplexen Nickelkatalysators | |
| AT259221B (de) | Verfahren zur Oligomerisation und Polymerisation von Olefinen | |
| DE2306624A1 (de) | Verfahren zur selektiven hydrierung von cyclischen butadienoligomeren | |
| CH459185A (de) | Verfahren zur Di- bzw. Trimerisation von 1,3-Diolefinen | |
| DE1204669B (de) | Verfahren zur Herstellung von Oligomeren von 1, 3-Dienen | |
| DE1133368B (de) | Verfahren zur Herstellung von niederen fluessigen Oligomeren aus 1, 3-Dienen |