JPH052657B2 - - Google Patents
Info
- Publication number
- JPH052657B2 JPH052657B2 JP61093352A JP9335286A JPH052657B2 JP H052657 B2 JPH052657 B2 JP H052657B2 JP 61093352 A JP61093352 A JP 61093352A JP 9335286 A JP9335286 A JP 9335286A JP H052657 B2 JPH052657 B2 JP H052657B2
- Authority
- JP
- Japan
- Prior art keywords
- reaction
- biphenyl
- ethylbiphenyl
- ethylbenzenes
- diethylbiphenyl
- 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.)
- Expired - Fee Related
Links
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 32
- 238000006243 chemical reaction Methods 0.000 claims description 27
- DLMYHUARHITGIJ-UHFFFAOYSA-N 1-ethyl-2-phenylbenzene Chemical group CCC1=CC=CC=C1C1=CC=CC=C1 DLMYHUARHITGIJ-UHFFFAOYSA-N 0.000 claims description 17
- 235000010290 biphenyl Nutrition 0.000 claims description 16
- 239000004305 biphenyl Substances 0.000 claims description 16
- 150000005194 ethylbenzenes Chemical class 0.000 claims description 15
- UMSGIWAAMHRVQI-UHFFFAOYSA-N 1-ethyl-4-(4-ethylphenyl)benzene Chemical group C1=CC(CC)=CC=C1C1=CC=C(CC)C=C1 UMSGIWAAMHRVQI-UHFFFAOYSA-N 0.000 claims description 14
- 239000002994 raw material Substances 0.000 claims description 10
- 238000010555 transalkylation reaction Methods 0.000 claims description 10
- 239000007795 chemical reaction product Substances 0.000 claims description 7
- 238000004821 distillation Methods 0.000 claims description 6
- 238000005727 Friedel-Crafts reaction Methods 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000000047 product Substances 0.000 claims description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 12
- ZVEJRZRAUYJYCO-UHFFFAOYSA-N 9-methyl-9h-fluorene Chemical compound C1=CC=C2C(C)C3=CC=CC=C3C2=C1 ZVEJRZRAUYJYCO-UHFFFAOYSA-N 0.000 description 9
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 description 8
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 8
- 239000006227 byproduct Substances 0.000 description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- VIDOPANCAUPXNH-UHFFFAOYSA-N 1,2,3-triethylbenzene Chemical compound CCC1=CC=CC(CC)=C1CC VIDOPANCAUPXNH-UHFFFAOYSA-N 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- AYDIPERXFQBZQX-UHFFFAOYSA-N 1,2,3-triethyl-4-phenylbenzene Chemical group CCC1=C(CC)C(CC)=CC=C1C1=CC=CC=C1 AYDIPERXFQBZQX-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- -1 ethyl-substituted benzene Chemical class 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- PBWHJRFXUPLZDS-UHFFFAOYSA-N (1-Ethylpropyl)benzene Chemical compound CCC(CC)C1=CC=CC=C1 PBWHJRFXUPLZDS-UHFFFAOYSA-N 0.000 description 1
- FEWANSQOXSIFOK-UHFFFAOYSA-N 1,2,3,4-tetraethylbenzene Chemical compound CCC1=CC=C(CC)C(CC)=C1CC FEWANSQOXSIFOK-UHFFFAOYSA-N 0.000 description 1
- HYFLWBNQFMXCPA-UHFFFAOYSA-N 1-ethyl-2-methylbenzene Chemical compound CCC1=CC=CC=C1C HYFLWBNQFMXCPA-UHFFFAOYSA-N 0.000 description 1
- SRQOBNUBCLPPPH-UHFFFAOYSA-N 1-ethyl-4-phenylbenzene Chemical group C1=CC(CC)=CC=C1C1=CC=CC=C1 SRQOBNUBCLPPPH-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61093352A JPS62252733A (ja) | 1986-04-24 | 1986-04-24 | エチルビフエニル類の製造方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61093352A JPS62252733A (ja) | 1986-04-24 | 1986-04-24 | エチルビフエニル類の製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62252733A JPS62252733A (ja) | 1987-11-04 |
| JPH052657B2 true JPH052657B2 (enrdf_load_html_response) | 1993-01-13 |
Family
ID=14079880
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61093352A Granted JPS62252733A (ja) | 1986-04-24 | 1986-04-24 | エチルビフエニル類の製造方法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62252733A (enrdf_load_html_response) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4943553A (en) * | 1986-12-25 | 1990-07-24 | Nippon Steel Chemical Co., Ltd. | Method of making ethylbiphenyls |
| US5670704A (en) * | 1990-06-26 | 1997-09-23 | Amoco Corporation | Selective production of 2,6-dimethylnaphthalene |
-
1986
- 1986-04-24 JP JP61093352A patent/JPS62252733A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62252733A (ja) | 1987-11-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP3022811B2 (ja) | シクロペンタジエン類 | |
| US2744150A (en) | Preparation of m- and p-diisopropylbenzene | |
| JPH052657B2 (enrdf_load_html_response) | ||
| US2418023A (en) | Catalytic reconstruction of hydrocarbons | |
| US2388758A (en) | Process of making primary alkylated benzenes and naphthalenes | |
| JPH04230226A (ja) | 接触的アルケニルベンゼン環化 | |
| US2436695A (en) | Alkylation process | |
| US4431854A (en) | Continuous preparation of ethylbenzene in a heterogeneous-phase reaction | |
| US3248443A (en) | Process for alkylating aromatic hydrocarbons | |
| JPS58172327A (ja) | クメン及び／又はポリイソプロピルベンゼンの製法 | |
| US2423401A (en) | Alkylation of isoparaffins | |
| US3132189A (en) | Preparation of 1, 2, 4, 5-tetrallkylbenzenes from pseudocumene and propylene | |
| US2886604A (en) | Preparation of compounds having a benzylbenzyl halide structure | |
| JP2763386B2 (ja) | トリメチルインダンの減量方法および該減量方法を含むクメンの製造方法 | |
| JPS6157812B2 (enrdf_load_html_response) | ||
| US2883438A (en) | Process for the preparation of paradiisopropylbenzene | |
| US3092672A (en) | Diarylethanes by reaction of aromatics with carbyl sulfate | |
| US2814652A (en) | Process for the preparation of tri-isopropyl-benzene | |
| US2480267A (en) | Production of bicycloalkyl aromatic compounds | |
| US2582434A (en) | Production of hydrocarbon drying | |
| US2371163A (en) | Manufacture of aromatic compounds | |
| US2394810A (en) | Production of branched chain hydrocarbons | |
| SU729175A1 (ru) | Способ получени алкилбензолов | |
| JPS585234B2 (ja) | ゴウセイタンカスイソジユンカツザイソセイブツノ セイゾウホウホウ | |
| US2397542A (en) | Alkylation |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |