DE2206971A1 - Verfahren zur Isomerisierung von Dichlorbutenen - Google Patents
Verfahren zur Isomerisierung von DichlorbutenenInfo
- Publication number
- DE2206971A1 DE2206971A1 DE19722206971 DE2206971A DE2206971A1 DE 2206971 A1 DE2206971 A1 DE 2206971A1 DE 19722206971 DE19722206971 DE 19722206971 DE 2206971 A DE2206971 A DE 2206971A DE 2206971 A1 DE2206971 A1 DE 2206971A1
- Authority
- DE
- Germany
- Prior art keywords
- dichlorobutene
- copper
- isomerization
- chlorine
- catalyst
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 16
- 238000006317 isomerization reaction Methods 0.000 title claims description 12
- UAZUEJTXWAXSMA-UHFFFAOYSA-N 1,1-dichlorobut-1-ene Chemical class CCC=C(Cl)Cl UAZUEJTXWAXSMA-UHFFFAOYSA-N 0.000 title claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 22
- 239000003054 catalyst Substances 0.000 claims description 19
- XVEASTGLHPVZNA-UHFFFAOYSA-N 3,4-dichlorobut-1-ene Chemical compound ClCC(Cl)C=C XVEASTGLHPVZNA-UHFFFAOYSA-N 0.000 claims description 15
- FQDIANVAWVHZIR-OWOJBTEDSA-N trans-1,4-Dichlorobutene Chemical compound ClC\C=C\CCl FQDIANVAWVHZIR-OWOJBTEDSA-N 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 11
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 7
- 229910052801 chlorine Inorganic materials 0.000 claims description 7
- 239000000460 chlorine Substances 0.000 claims description 7
- 229910052802 copper Inorganic materials 0.000 claims description 7
- 239000010949 copper Substances 0.000 claims description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 claims description 5
- 239000005749 Copper compound Substances 0.000 claims description 4
- 150000001880 copper compounds Chemical class 0.000 claims description 4
- SVOAENZIOKPANY-CVBJKYQLSA-L copper;(z)-octadec-9-enoate Chemical compound [Cu+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O SVOAENZIOKPANY-CVBJKYQLSA-L 0.000 claims description 3
- PEVZEFCZINKUCG-UHFFFAOYSA-L copper;octadecanoate Chemical compound [Cu+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O PEVZEFCZINKUCG-UHFFFAOYSA-L 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 3
- 150000007522 mineralic acids Chemical class 0.000 claims 1
- DADSZOFTIIETSV-UHFFFAOYSA-N n,n-dichloroaniline Chemical compound ClN(Cl)C1=CC=CC=C1 DADSZOFTIIETSV-UHFFFAOYSA-N 0.000 claims 1
- 150000007524 organic acids Chemical class 0.000 claims 1
- 235000005985 organic acids Nutrition 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 238000009835 boiling Methods 0.000 description 6
- 239000000654 additive Substances 0.000 description 5
- QSNSCYSYFYORTR-UHFFFAOYSA-N 4-chloroaniline Chemical compound NC1=CC=C(Cl)C=C1 QSNSCYSYFYORTR-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- AVYGCQXNNJPXSS-UHFFFAOYSA-N 2,5-dichloroaniline Chemical compound NC1=CC(Cl)=CC=C1Cl AVYGCQXNNJPXSS-UHFFFAOYSA-N 0.000 description 3
- 150000001448 anilines Chemical class 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005194 fractionation Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229940049964 oleate Drugs 0.000 description 2
- SWSOIFQIPTXLOI-HNQUOIGGSA-N (e)-1,4-dichlorobut-1-ene Chemical compound ClCC\C=C\Cl SWSOIFQIPTXLOI-HNQUOIGGSA-N 0.000 description 1
- BRPSAOUFIJSKOT-UHFFFAOYSA-N 2,3-dichloroaniline Chemical compound NC1=CC=CC(Cl)=C1Cl BRPSAOUFIJSKOT-UHFFFAOYSA-N 0.000 description 1
- KQCMTOWTPBNWDB-UHFFFAOYSA-N 2,4-dichloroaniline Chemical compound NC1=CC=C(Cl)C=C1Cl KQCMTOWTPBNWDB-UHFFFAOYSA-N 0.000 description 1
- JDMFXJULNGEPOI-UHFFFAOYSA-N 2,6-dichloroaniline Chemical compound NC1=C(Cl)C=CC=C1Cl JDMFXJULNGEPOI-UHFFFAOYSA-N 0.000 description 1
- FCDOETBDFXHVJZ-UHFFFAOYSA-N 2-aminobenzoic acid;4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1.NC1=CC=CC=C1C(O)=O FCDOETBDFXHVJZ-UHFFFAOYSA-N 0.000 description 1
- MZZATKZTTVRCNA-UHFFFAOYSA-N 2-chloroaniline;3-chloroaniline Chemical compound NC1=CC=CC(Cl)=C1.NC1=CC=CC=C1Cl MZZATKZTTVRCNA-UHFFFAOYSA-N 0.000 description 1
- 241001026509 Kata Species 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical class [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical class [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical class [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- -1 aniline compound Chemical class 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 125000003963 dichloro group Chemical group Cl* 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000010936 titanium Chemical class 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000011701 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0231—Halogen-containing compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
- B01J31/0235—Nitrogen containing compounds
- B01J31/0237—Amines
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
- B01J31/0271—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds also containing elements or functional groups covered by B01J31/0201 - B01J31/0231
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/04—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
- B01J31/28—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of the platinum group metals, iron group metals or copper
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/50—Catalysts, in general, characterised by their form or physical properties characterised by their shape or configuration
- B01J35/51—Spheres
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/35—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction
- C07C17/358—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction by isomerisation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/50—Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
- B01J2231/52—Isomerisation reactions
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB471271 | 1971-02-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE2206971A1 true DE2206971A1 (de) | 1972-08-31 |
Family
ID=9782373
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19722206971 Pending DE2206971A1 (de) | 1971-02-16 | 1972-02-14 | Verfahren zur Isomerisierung von Dichlorbutenen |
Country Status (7)
Country | Link |
---|---|
JP (1) | JPS5613698B1 (fr) |
BE (1) | BE779407A (fr) |
DE (1) | DE2206971A1 (fr) |
FR (1) | FR2125438A1 (fr) |
GB (1) | GB1327983A (fr) |
IT (1) | IT965038B (fr) |
NL (1) | NL7202013A (fr) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2004880B (en) * | 1977-09-30 | 1982-07-14 | Denki Kagaku Kogyo Kk | Isomerization of dichlorobutenes |
JPS5692225A (en) | 1979-12-25 | 1981-07-25 | Denki Kagaku Kogyo Kk | Isomerizing method of dichlorobutene |
JPS5886399A (ja) * | 1981-11-18 | 1983-05-23 | Shinwa Sangyo Kk | 冷却塔 |
JPS6064185A (ja) * | 1983-09-16 | 1985-04-12 | Hitachi Reinetsu Jiyuusetsu Kk | ク−リングタワ−の白煙防止方法 |
JPH0554472U (ja) * | 1991-12-26 | 1993-07-20 | 古河機械金属株式会社 | コイルチューブの巻付け装置 |
-
1971
- 1971-02-16 GB GB471271A patent/GB1327983A/en not_active Expired
-
1972
- 1972-02-14 JP JP1550972A patent/JPS5613698B1/ja active Pending
- 1972-02-14 FR FR7204797A patent/FR2125438A1/fr not_active Withdrawn
- 1972-02-14 DE DE19722206971 patent/DE2206971A1/de active Pending
- 1972-02-15 IT IT20600/72A patent/IT965038B/it active
- 1972-02-15 BE BE779407A patent/BE779407A/fr unknown
- 1972-02-16 NL NL7202013A patent/NL7202013A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
FR2125438A1 (fr) | 1972-09-29 |
IT965038B (it) | 1974-01-31 |
NL7202013A (fr) | 1972-08-18 |
GB1327983A (en) | 1973-08-22 |
BE779407A (fr) | 1972-08-16 |
JPS5613698B1 (fr) | 1981-03-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1398305A1 (fr) | Procédé pour la déshydrochloration d' ortho-xylènes chlorés dans le noyau | |
DE2615079A1 (de) | Verfahren zur katalytischen reduktion von halogensubstituierten mononitroaromatischen kohlenwasserstoffen | |
DE2206971A1 (de) | Verfahren zur Isomerisierung von Dichlorbutenen | |
DE2107468A1 (de) | Verfahren zur Isomerisation von 1,4 Dichlorbuten 2 und 3,4 Dichlorbuten 1 | |
DE1443079A1 (de) | Verfahren zur Herstellung von 1,2-Dichloraethan | |
DE926185C (de) | Verfahren zur Herstellung von m-Dichlorbenzol aus o- oder p-Dichlorbenzol oder einemGemisch der Dichlorbenzole | |
EP0073987B1 (fr) | Procédé de préparation de 1,3,5-trichlorobenzène | |
DE2130488C3 (de) | Verfahren zur Isomerisation von l,4-Dichlorbuten-<2) in 3,4-Dichlorbuten-(1) und umgekehrt | |
DE891841C (de) | Verfahren zur Herstellung von Hexachlorbenzol | |
DE2212235A1 (de) | Verfahren zur Isomerisierung von Dichlorbutenen | |
DE2842610C3 (de) | Verfahren zur Isomerisierung zwischen 3,4-Dichlorbuten - (1) und 1,4 -Dichlorbuten - (2) | |
DE727626C (de) | Verfahren zur Herstellung von Cyclohexanol neben Cyclohexanon | |
DE626923C (de) | Verfahren zur UEberfuehrung von sekundaeren und tertiaeren Aminen in niedrigere Substitutionsstufen | |
DE2200780C3 (de) | Verfahren zur Isomerisation von 3,4-Dichlorbuten-(1) bzw. von 1,4-Dichlorbuten-(2) | |
DE2010209A1 (fr) | ||
DE2256167B1 (fr) | ||
CH619914A5 (en) | Process for the continuous preparation of o- and p-chlorotoluene. | |
DE700434C (fr) | ||
DE864865C (de) | Verfahren zur Herstellung von ª€-Heptachlorcyclohexan aus Benzol | |
DE1768427C2 (de) | Verfahren zur Herstellung eines im Gleichgewicht oder nahezu im Gleichgewicht befindlichen Isomerengemisches von Bis-(p-aminocyclohexyl)-methan aus einem Stereoisomeren oder einem nicht im Gleichgewicht befindlichen Isomerengemisch | |
DE949655C (de) | Verfahren zur katalytischen Chlorwasserstoffabspaltung aus Hexachlorcyclohexan | |
DE937050C (de) | Verfahren zur Herstellung von 1, 3, 5-Cycloheptatrienen | |
DE1618175A1 (de) | Verfahren zur Herstellung von technischen Trichlorbenzol | |
DE976461C (de) | Verfahren zur Chlorierung von gesaettigten oder ungesaettigten aliphatischen und cycloaliphatischen oder von aromatischen Kohlenwasserstoffen mit elementarem Chlor | |
DE2138790A1 (de) | Verfahren zur Isomerisierung von Dichlorbutenen |