NL7908227A - Werkwijze voor de bereiding van omzettingsprodukten van geconjugeerde dialkenen en aromatische koolwater- stoffen. - Google Patents

Werkwijze voor de bereiding van omzettingsprodukten van geconjugeerde dialkenen en aromatische koolwater- stoffen. Download PDF

Info

Publication number: NL7908227A
Authority: NL; Netherlands
Prior art keywords: halogen; optionally; atoms; aromatic hydrocarbons; conjugated
Prior art date: 1978-11-10

Application number

NL7908227A

Other languages

English (en)

Dutch (nl)

Original Assignee

Huels Chemische Werke Ag

Priority date (The priority date 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 date listed.)

1978-11-10

Filing date

1979-11-09

Publication date

1980-05-13

1979-11-09 Application filed by Huels Chemische Werke Ag filed Critical Huels Chemische Werke Ag

1980-05-13 Publication of NL7908227A publication Critical patent/NL7908227A/nl

Links

150000004945 aromatic hydrocarbons Chemical class 0.000 title claims description 15
239000012084 conversion product Substances 0.000 title claims description 7
238000004519 manufacturing process Methods 0.000 title 1
238000000034 method Methods 0.000 claims description 18
-1 aluminum organic compound Chemical class 0.000 claims description 15
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 13
150000001993 dienes Chemical class 0.000 claims description 13
229910052740 iodine Inorganic materials 0.000 claims description 13
125000003118 aryl group Chemical group 0.000 claims description 11
229910052736 halogen Inorganic materials 0.000 claims description 11
150000002367 halogens Chemical class 0.000 claims description 11
229910052782 aluminium Inorganic materials 0.000 claims description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 6
239000003054 catalyst Substances 0.000 claims description 6
150000001875 compounds Chemical class 0.000 claims description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
239000003795 chemical substances by application Substances 0.000 claims description 5
150000002816 nickel compounds Chemical class 0.000 claims description 5
239000000460 chlorine Substances 0.000 claims description 4
238000002360 preparation method Methods 0.000 claims description 4
229920006395 saturated elastomer Polymers 0.000 claims description 4
125000004417 unsaturated alkyl group Chemical group 0.000 claims description 4
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 3
229910052794 bromium Inorganic materials 0.000 claims description 3
229910052799 carbon Inorganic materials 0.000 claims description 3
229910052801 chlorine Inorganic materials 0.000 claims description 3
125000005843 halogen group Chemical group 0.000 claims description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
125000004429 atom Chemical group 0.000 claims 1
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 27
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 12
238000006243 chemical reaction Methods 0.000 description 12
239000000047 product Substances 0.000 description 11
239000011630 iodine Substances 0.000 description 10
239000003607 modifier Substances 0.000 description 7
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
YTKRILODNOEEPX-NSCUHMNNSA-N crotyl chloride Chemical compound C\C=C\CCl YTKRILODNOEEPX-NSCUHMNNSA-N 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
238000001228 spectrum Methods 0.000 description 4
VFWCMGCRMGJXDK-UHFFFAOYSA-N 1-chlorobutane Chemical compound CCCCCl VFWCMGCRMGJXDK-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical class [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 description 3
238000004061 bleaching Methods 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
229920002554 vinyl polymer Polymers 0.000 description 3
238000010626 work up procedure Methods 0.000 description 3
SQCZQTSHSZLZIQ-UHFFFAOYSA-N 1-chloropentane Chemical compound CCCCCCl SQCZQTSHSZLZIQ-UHFFFAOYSA-N 0.000 description 2
SDJHPPZKZZWAKF-UHFFFAOYSA-N 2,3-dimethylbuta-1,3-diene Chemical compound CC(=C)C(C)=C SDJHPPZKZZWAKF-UHFFFAOYSA-N 0.000 description 2
UVPKUTPZWFHAHY-UHFFFAOYSA-L 2-ethylhexanoate;nickel(2+) Chemical compound [Ni+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O UVPKUTPZWFHAHY-UHFFFAOYSA-L 0.000 description 2
CMAOLVNGLTWICC-UHFFFAOYSA-N 2-fluoro-5-methylbenzonitrile Chemical compound CC1=CC=C(F)C(C#N)=C1 CMAOLVNGLTWICC-UHFFFAOYSA-N 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
238000007605 air drying Methods 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
125000001246 bromo group Chemical group Br* 0.000 description 2
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
150000002366 halogen compounds Chemical class 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
238000005984 hydrogenation reaction Methods 0.000 description 2
239000000203 mixture Substances 0.000 description 2
229920002857 polybutadiene Polymers 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical group C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
238000005160 1H NMR spectroscopy Methods 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
OHXAOPZTJOUYKM-UHFFFAOYSA-N 3-Chloro-2-methylpropene Chemical compound CC(=C)CCl OHXAOPZTJOUYKM-UHFFFAOYSA-N 0.000 description 1
OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 1
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-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
KUGRPPRAQNPSQD-UHFFFAOYSA-N OOOOO Chemical compound OOOOO KUGRPPRAQNPSQD-UHFFFAOYSA-N 0.000 description 1
239000005062 Polybutadiene Substances 0.000 description 1
238000001069 Raman spectroscopy Methods 0.000 description 1
241000220317 Rosa Species 0.000 description 1
MPMBRWOOISTHJV-XVNBXDOJSA-N [(e)-but-1-enyl]benzene Chemical compound CC\C=C\C1=CC=CC=C1 MPMBRWOOISTHJV-XVNBXDOJSA-N 0.000 description 1
ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
150000007514 bases Chemical class 0.000 description 1
AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 1
KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
229940073608 benzyl chloride Drugs 0.000 description 1
238000009835 boiling Methods 0.000 description 1
150000001649 bromium compounds Chemical class 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
238000000576 coating method Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
230000001268 conjugating effect Effects 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000003599 detergent Substances 0.000 description 1
235000001916 dieting Nutrition 0.000 description 1
230000037228 dieting effect Effects 0.000 description 1
238000004821 distillation Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
238000005194 fractionation Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
230000026030 halogenation Effects 0.000 description 1
238000005658 halogenation reaction Methods 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
150000004694 iodide salts Chemical class 0.000 description 1
125000002346 iodo group Chemical group I* 0.000 description 1
238000002955 isolation Methods 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
239000002808 molecular sieve Substances 0.000 description 1
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
UIEKYBOPAVTZKW-UHFFFAOYSA-L naphthalene-2-carboxylate;nickel(2+) Chemical compound [Ni+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 UIEKYBOPAVTZKW-UHFFFAOYSA-L 0.000 description 1
JMWUYEFBFUCSAK-UHFFFAOYSA-L nickel(2+);octadecanoate Chemical compound [Ni+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O JMWUYEFBFUCSAK-UHFFFAOYSA-L 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
230000002250 progressing effect Effects 0.000 description 1
238000000746 purification Methods 0.000 description 1
239000002994 raw material Substances 0.000 description 1
238000007086 side reaction Methods 0.000 description 1
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
102000055501 telomere Human genes 0.000 description 1
108091035539 telomere Proteins 0.000 description 1
210000003411 telomere Anatomy 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
238000012360 testing method Methods 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
150000003613 toluenes Chemical class 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/54—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
- C07C2/72—Addition to a non-aromatic carbon atom of hydrocarbons containing a six-membered aromatic ring
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/38—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
- C08F236/10—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated with vinyl-aromatic monomers
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- C07C2531/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
- C07C2531/14—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

NL7908227A 1978-11-10 1979-11-09 Werkwijze voor de bereiding van omzettingsprodukten van geconjugeerde dialkenen en aromatische koolwater- stoffen. NL7908227A (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE2848804		1978-11-10
DE19782848804 DE2848804A1 (de)	1978-11-10	1978-11-10	Verfahren zur herstellung von reaktionsprodukten aus konjugierten diolefinen und aromatischen kohlenwasserstoffen

Publications (1)

Publication Number	Publication Date
NL7908227A true NL7908227A (nl)	1980-05-13

Family

ID=6054337

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL7908227A NL7908227A (nl)	1978-11-10	1979-11-09	Werkwijze voor de bereiding van omzettingsprodukten van geconjugeerde dialkenen en aromatische koolwater- stoffen.

Country Status (8)

Country	Link
US (1)	US4284836A (fr)
JP (1)	JPS5566528A (fr)
BE (1)	BE879940A (fr)
DE (1)	DE2848804A1 (fr)
FR (1)	FR2453841A1 (fr)
GB (1)	GB2037313B (fr)
IT (1)	IT7950796A0 (fr)
NL (1)	NL7908227A (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3000708A1 (de) *	1980-01-10	1981-07-16	Chemische Werke Hüls AG, 4370 Marl	Verfahren zur herstellung von reaktionsprodukten aus konjugierten diolefinen und aromatischen kohlenwasserstoffen
US5281368A (en) *	1992-03-31	1994-01-25	Exxon Chemical Patents Inc.	Norbornene polymerization initiators and process for preparing same

1978
- 1978-11-10 DE DE19782848804 patent/DE2848804A1/de not_active Withdrawn
1979
- 1979-11-06 US US06/091,909 patent/US4284836A/en not_active Expired - Lifetime
- 1979-11-06 FR FR7927355A patent/FR2453841A1/fr not_active Withdrawn
- 1979-11-09 NL NL7908227A patent/NL7908227A/nl not_active Application Discontinuation
- 1979-11-09 JP JP14456479A patent/JPS5566528A/ja active Pending
- 1979-11-09 IT IT7950796A patent/IT7950796A0/it unknown
- 1979-11-09 BE BE0/198053A patent/BE879940A/fr unknown
- 1979-11-09 GB GB7938829A patent/GB2037313B/en not_active Expired

Also Published As

Publication number	Publication date
GB2037313A (en)	1980-07-09
US4284836A (en)	1981-08-18
GB2037313B (en)	1982-10-13
DE2848804A1 (de)	1980-05-22
JPS5566528A (en)	1980-05-20
BE879940A (fr)	1980-05-09
IT7950796A0 (it)	1979-11-09
FR2453841A1 (fr)	1980-11-07

Legal Events

Date	Code	Title	Description
1983-07-01	BV	The patent application has lapsed

Publication	Publication Date	Title
Alderson et al.	1965	Olefin-to-olefin addition reactions
US3013066A (en)	1961-12-12	Dimerization of alpha olefins with a group viii noble metal salt
US9862906B2 (en)	2018-01-09	Base oils and methods for making the same
US8865959B2 (en)	2014-10-21	Process for synthetic lubricant production
Grieco et al.	1975	Sesterterpenes. I. Stereospecific total synthesis of moenocinol
DE671419T1 (de)	1996-09-19	Herstellung von Polybutenen.
JPS5922687B2 (ja)	1984-05-28	ブテン−１の重合体の製法
DE69219291T2 (de)	1997-11-20	Verfahren zur Hydrierung von Verbindungen mit olefinischer Ungesättigtkeit
NL7908227A (nl)	1980-05-13	Werkwijze voor de bereiding van omzettingsprodukten van geconjugeerde dialkenen en aromatische koolwater- stoffen.
HUE030225T2 (en)	2017-04-28	A method of producing branched polybutadiene having a high 1,4-cis unit content
US4324939A (en)	1982-04-13	Process for preparing reaction products of conjugated diolefins and aromatic hydrocarbons
Hoyte et al.	1974	Cis-trans isomerization of allylic radicals
Smith et al.	1961	The kolbe electrolysis as a source of free radicals in solution. III. Some aspects of the stereochemistry of the electrode process
JPH0694556B2 (ja)	1994-11-24	食品加工機械用潤滑油組成物
EP0020913B1 (fr)	1983-03-09	Copolymères de polybutadiène et d'alpha oléfines, et leur préparation
US2773799A (en)	1956-12-11	Compounds, preparation and fungicidal compositions of polyhalogeno alkyl polycyclyl ketones
DE1299874B (de)	1969-07-24	Verfahren zur Herstellung von mit Schwefel vulkanisierbaren, elastomeren Copolymerisaten aus AEthylen, Propylen und Trienen
DE2133584A1 (de)	1972-02-03	Kohlenwasserstoffe
Carlini et al.	2001	Catalytic performances of homogeneous systems based on α-nitroacetophenonate-nickel (II) complexes and organoaluminium compounds in ethylene oligomerisation
CH462148A (de)	1968-09-15	Verfahren zur Herstellung von Zyklododekatrienen-1,5,9
Nelson et al.	1983	Synthetic lubricants: star-branched oligomers via metathesis/dimerization of 1-octene and or 1-decene
EP0075234B1 (fr)	1984-09-12	Esters d'acides acyloxyalcadiène carboxyliques et procédé de préparation
CH411836A (de)	1966-04-30	Verfahren zur Herstellung von Mischoligomeren aus 1,3-Dienen und Verbindungen mit aktivierter olefinischer Doppelbindung
DE1418352C (de)	1971-08-26	Verfahren zur katalytischen Codimen sation alpha olefinartiger Verbindungen
DE1593574C3 (de)	1976-05-13	Verfahren zur Herstellung von Hexadienen