JPS58210039A - 第３級ブチルアルキルエ−テルの製法 - Google Patents
第３級ブチルアルキルエ−テルの製法Info
- Publication number
- JPS58210039A JPS58210039A JP58087816A JP8781683A JPS58210039A JP S58210039 A JPS58210039 A JP S58210039A JP 58087816 A JP58087816 A JP 58087816A JP 8781683 A JP8781683 A JP 8781683A JP S58210039 A JPS58210039 A JP S58210039A
- Authority
- JP
- Japan
- Prior art keywords
- butene
- alkyl ether
- hydrocarbon
- tertiary butyl
- raw material
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 title description 4
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 49
- 229930195733 hydrocarbon Natural products 0.000 claims description 28
- 150000002430 hydrocarbons Chemical class 0.000 claims description 28
- 239000004215 Carbon black (E152) Substances 0.000 claims description 25
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims description 25
- 239000002994 raw material Substances 0.000 claims description 14
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 claims description 14
- -1 butyl alkyl ether Chemical group 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 12
- 238000006317 isomerization reaction Methods 0.000 claims description 10
- 230000015572 biosynthetic process Effects 0.000 claims description 8
- 238000003786 synthesis reaction Methods 0.000 claims description 8
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 5
- XNMQEEKYCVKGBD-UHFFFAOYSA-N dimethylacetylene Natural products CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 claims description 4
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 239000003456 ion exchange resin Substances 0.000 claims description 3
- 229920003303 ion-exchange polymer Polymers 0.000 claims description 3
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- SZNYYWIUQFZLLT-UHFFFAOYSA-N 2-methyl-1-(2-methylpropoxy)propane Chemical compound CC(C)COCC(C)C SZNYYWIUQFZLLT-UHFFFAOYSA-N 0.000 claims 2
- 102100033227 Teneurin-2 Human genes 0.000 claims 1
- 101710122316 Teneurin-2 Proteins 0.000 claims 1
- 150000005215 alkyl ethers Chemical class 0.000 claims 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 239000001282 iso-butane Substances 0.000 description 3
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- CHRJZRDFSQHIFI-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;styrene Chemical class C=CC1=CC=CC=C1.C=CC1=CC=CC=C1C=C CHRJZRDFSQHIFI-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004230 steam cracking Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/04—Saturated ethers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/05—Preparation of ethers by addition of compounds to unsaturated compounds
- C07C41/06—Preparation of ethers by addition of compounds to unsaturated compounds by addition of organic compounds only
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT21384/82A IT1151183B (it) | 1982-05-20 | 1982-05-20 | Procedimento per la produzione di eteri alchil ter-butilici |
| IT21384A/82 | 1982-05-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS58210039A true JPS58210039A (ja) | 1983-12-07 |
Family
ID=11180967
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58087816A Pending JPS58210039A (ja) | 1982-05-20 | 1983-05-20 | 第３級ブチルアルキルエ−テルの製法 |
Country Status (30)
| Country | Link |
|---|---|
| JP (1) | JPS58210039A (enExample) |
| KR (1) | KR860001854B1 (enExample) |
| AU (1) | AU1401783A (enExample) |
| BE (1) | BE896787A (enExample) |
| BG (1) | BG37678A3 (enExample) |
| BR (1) | BR8302433A (enExample) |
| CA (1) | CA1220230A (enExample) |
| CH (1) | CH653664A5 (enExample) |
| DD (1) | DD209803A5 (enExample) |
| DE (1) | DE3318301A1 (enExample) |
| DK (1) | DK221683A (enExample) |
| ES (1) | ES523006A0 (enExample) |
| FR (1) | FR2527202B1 (enExample) |
| GB (1) | GB2121407B (enExample) |
| GR (1) | GR78857B (enExample) |
| IN (1) | IN159788B (enExample) |
| IT (1) | IT1151183B (enExample) |
| LU (1) | LU84805A1 (enExample) |
| MW (1) | MW1883A1 (enExample) |
| NL (1) | NL8301819A (enExample) |
| NO (1) | NO831759L (enExample) |
| NZ (1) | NZ204032A (enExample) |
| PH (1) | PH19481A (enExample) |
| PL (1) | PL242093A1 (enExample) |
| PT (1) | PT76730B (enExample) |
| SE (1) | SE8302577L (enExample) |
| TR (1) | TR21617A (enExample) |
| YU (1) | YU110083A (enExample) |
| ZA (1) | ZA833068B (enExample) |
| ZW (1) | ZW9783A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06279340A (ja) * | 1993-01-06 | 1994-10-04 | Stone & Webster Eng Corp | 統合ｍｔｂｅプロセス |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4731490A (en) * | 1986-07-23 | 1988-03-15 | Arco Chemical Company | Process for methyl, tertiary butyl ether production |
| FR2614297B1 (fr) * | 1987-04-24 | 1989-07-21 | Inst Francais Du Petrole | Procede de production de methyl-tertiobutyl-ether a partir de n-butenes. |
| FR2710907B1 (fr) * | 1993-10-08 | 1996-01-05 | Inst Francais Du Petrole | Procédé de production d'éthers tertiaires à partir d'une charge de craquage catalytique comprenant deux étapes de distillation extractive. |
| IT1270675B (it) | 1994-10-19 | 1997-05-07 | Enichem Spa | Procedimento per la separazione di paraffine in miscela con olefine |
| CN103755512B (zh) * | 2013-12-24 | 2016-01-06 | 山东滨州裕华化工厂有限公司 | 醚后液化气分离c4馏分的工艺 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1224294B (de) * | 1961-01-09 | 1966-09-08 | Bayer Ag | Verfahren zur Herstellung von tertiaeren Butylalkylaethern |
| FR2455019A1 (fr) * | 1979-04-24 | 1980-11-21 | Inst Francais Du Petrole | Procede de production de methyltertiobutyl ether a partir de methanol et d'isobutene |
| DE2921576A1 (de) * | 1979-05-28 | 1980-12-04 | Davy International Ag | Verfahren zur herstellung von methyl-tert.-butylaether |
-
1982
- 1982-05-20 IT IT21384/82A patent/IT1151183B/it active
-
1983
- 1983-04-28 AU AU14017/83A patent/AU1401783A/en not_active Abandoned
- 1983-04-28 NZ NZ204032A patent/NZ204032A/en unknown
- 1983-04-28 GR GR71241A patent/GR78857B/el unknown
- 1983-04-29 ZW ZW97/83A patent/ZW9783A1/xx unknown
- 1983-04-29 ZA ZA833068A patent/ZA833068B/xx unknown
- 1983-05-05 SE SE8302577A patent/SE8302577L/ not_active Application Discontinuation
- 1983-05-05 CH CH2465/83A patent/CH653664A5/it not_active IP Right Cessation
- 1983-05-06 BR BR8302433A patent/BR8302433A/pt unknown
- 1983-05-12 GB GB08313098A patent/GB2121407B/en not_active Expired
- 1983-05-13 KR KR1019830002066A patent/KR860001854B1/ko not_active Expired
- 1983-05-13 LU LU84805A patent/LU84805A1/fr unknown
- 1983-05-13 MW MW18/83A patent/MW1883A1/xx unknown
- 1983-05-17 YU YU01100/83A patent/YU110083A/xx unknown
- 1983-05-17 FR FR8308163A patent/FR2527202B1/fr not_active Expired
- 1983-05-18 PH PH28926A patent/PH19481A/en unknown
- 1983-05-18 BG BG061013A patent/BG37678A3/xx unknown
- 1983-05-18 DK DK221683A patent/DK221683A/da not_active Application Discontinuation
- 1983-05-18 TR TR21617A patent/TR21617A/xx unknown
- 1983-05-18 NO NO831759A patent/NO831759L/no unknown
- 1983-05-19 CA CA000428516A patent/CA1220230A/en not_active Expired
- 1983-05-19 BE BE0/210806A patent/BE896787A/fr not_active IP Right Cessation
- 1983-05-19 PT PT76730A patent/PT76730B/pt unknown
- 1983-05-19 DD DD83251077A patent/DD209803A5/de unknown
- 1983-05-19 DE DE19833318301 patent/DE3318301A1/de not_active Withdrawn
- 1983-05-20 NL NL8301819A patent/NL8301819A/nl not_active Application Discontinuation
- 1983-05-20 JP JP58087816A patent/JPS58210039A/ja active Pending
- 1983-05-20 PL PL24209383A patent/PL242093A1/xx unknown
- 1983-05-20 IN IN632/CAL/83A patent/IN159788B/en unknown
- 1983-05-20 ES ES523006A patent/ES523006A0/es active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06279340A (ja) * | 1993-01-06 | 1994-10-04 | Stone & Webster Eng Corp | 統合ｍｔｂｅプロセス |
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