JP2004536147A - イソプロパノールの製造方法 - Google Patents
イソプロパノールの製造方法 Download PDFInfo
- Publication number
- JP2004536147A JP2004536147A JP2003516996A JP2003516996A JP2004536147A JP 2004536147 A JP2004536147 A JP 2004536147A JP 2003516996 A JP2003516996 A JP 2003516996A JP 2003516996 A JP2003516996 A JP 2003516996A JP 2004536147 A JP2004536147 A JP 2004536147A
- Authority
- JP
- Japan
- Prior art keywords
- benzene
- isopropanol
- acetone
- product
- 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
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 title claims abstract description 120
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 11
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims abstract description 136
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical class CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims abstract description 107
- 238000000034 method Methods 0.000 claims abstract description 43
- 239000002994 raw material Substances 0.000 claims abstract description 11
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 9
- 150000004678 hydrides Chemical class 0.000 claims abstract 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 49
- 239000003054 catalyst Substances 0.000 claims description 37
- 239000000047 product Substances 0.000 claims description 29
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 claims description 25
- 229910052759 nickel Inorganic materials 0.000 claims description 23
- 239000006227 byproduct Substances 0.000 claims description 19
- 238000005984 hydrogenation reaction Methods 0.000 claims description 19
- 239000007788 liquid Substances 0.000 claims description 19
- 239000001257 hydrogen Substances 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
- 239000007795 chemical reaction product Substances 0.000 claims description 11
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 claims description 5
- -1 benzene contaminated acetone Chemical class 0.000 claims description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 4
- 230000002152 alkylating effect Effects 0.000 claims description 2
- 230000001590 oxidative effect Effects 0.000 claims description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 230000003134 recirculating effect Effects 0.000 claims description 2
- 238000000926 separation method Methods 0.000 abstract description 9
- 238000004821 distillation Methods 0.000 description 21
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 14
- 239000007789 gas Substances 0.000 description 11
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- 239000000377 silicon dioxide Substances 0.000 description 7
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 238000004064 recycling Methods 0.000 description 6
- 238000010543 cumene process Methods 0.000 description 5
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 3
- 229940051250 hexylene glycol Drugs 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000003463 adsorbent Substances 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- JYVHOGDBFNJNMR-UHFFFAOYSA-N hexane;hydrate Chemical compound O.CCCCCC JYVHOGDBFNJNMR-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 150000001908 cumenes Chemical class 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052987 metal hydride Inorganic materials 0.000 description 1
- 150000004681 metal hydrides Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000004441 surface measurement Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/143—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of ketones
- C07C29/145—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of ketones with hydrogen or hydrogen-containing gases
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/88—Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound
- C07C29/90—Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound using hydrogen only
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring monocyclic with no unsaturation outside the aromatic ring
- C07C39/04—Phenol
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Steroid Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP01309673 | 2001-11-16 | ||
| PCT/EP2002/012650 WO2003011801A2 (en) | 2001-11-16 | 2002-11-12 | Process for the preparation of isopropanol |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004536147A true JP2004536147A (ja) | 2004-12-02 |
| JP2004536147A5 JP2004536147A5 (cg-RX-API-DMAC7.html) | 2009-09-24 |
Family
ID=8182464
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003516996A Pending JP2004536147A (ja) | 2001-11-16 | 2002-11-12 | イソプロパノールの製造方法 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US6939995B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP1463700B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2004536147A (cg-RX-API-DMAC7.html) |
| KR (1) | KR20040055805A (cg-RX-API-DMAC7.html) |
| CN (1) | CN1266100C (cg-RX-API-DMAC7.html) |
| AT (1) | ATE361270T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU2002342904A1 (cg-RX-API-DMAC7.html) |
| BR (1) | BR0214170A (cg-RX-API-DMAC7.html) |
| DE (1) | DE60219960T2 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2286298T3 (cg-RX-API-DMAC7.html) |
| MX (1) | MXPA04004553A (cg-RX-API-DMAC7.html) |
| RU (1) | RU2296740C2 (cg-RX-API-DMAC7.html) |
| TW (1) | TWI266762B (cg-RX-API-DMAC7.html) |
| WO (1) | WO2003011801A2 (cg-RX-API-DMAC7.html) |
| ZA (1) | ZA200402797B (cg-RX-API-DMAC7.html) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007038217A (ja) * | 2005-07-30 | 2007-02-15 | Oxeno Olefinchemie Gmbh | 水素化触媒及びエステル含有アルデヒド混合物の接触水素化法 |
| WO2008062644A1 (fr) * | 2006-11-21 | 2008-05-29 | Mitsui Chemicals, Inc. | Procédé de fabrication d'un composé aromatique alkylé et procédé de fabrication de phénol |
| JP2008285477A (ja) * | 2007-04-18 | 2008-11-27 | Mitsui Chemicals Inc | アルキル化芳香族化合物の製造方法およびフェノールの製造方法 |
| WO2014002884A1 (ja) * | 2012-06-27 | 2014-01-03 | 三井化学株式会社 | イソプロパノールの製造方法 |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10008924A1 (de) * | 2000-02-25 | 2001-09-06 | Phenolchemie Gmbh & Co Kg | Verfahren zur Herstellung von Phenol |
| TWI301480B (en) * | 2001-11-16 | 2008-10-01 | Shell Int Research | Process for the hydrogenation of acetone |
| KR100874774B1 (ko) * | 2006-08-21 | 2008-12-19 | 이수화학 주식회사 | 이소프로판올 및 고순도 노말파라핀의 동시 제조방법 |
| US7799958B2 (en) | 2007-10-04 | 2010-09-21 | Barclays Bank Plc | Process for the production of iso-propanol by liquid phase hydrogenation |
| KR20110082156A (ko) * | 2008-10-06 | 2011-07-18 | 바져 라이센싱 엘엘씨 | 큐멘의 제조방법 |
| CN102690172A (zh) * | 2011-03-25 | 2012-09-26 | 中国石油化工股份有限公司 | 丙酮加氢生产异丙醇的方法 |
| CN103539635B (zh) * | 2012-07-12 | 2016-07-13 | 中国石油化工股份有限公司 | 用于丙酮加氢制备异丙醇的方法 |
| CN109851467A (zh) * | 2012-07-26 | 2019-06-07 | 巴杰许可有限责任公司 | 制备枯烯的方法 |
| CN103772145B (zh) * | 2012-10-23 | 2016-09-21 | 中国石油化工股份有限公司 | 一种丙酮加氢制异丙醇的分离方法 |
| RU2519950C1 (ru) * | 2013-03-05 | 2014-06-20 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Волгоградский государственный технический университет" (ВолгГТУ) | Способ получения первичных или вторичный спиртов |
| CN106008186B (zh) * | 2016-06-02 | 2018-05-15 | 南京师范大学 | 一种异丙醇、丙酮及水混合溶液的分离方法 |
| EP4488252A1 (en) * | 2022-08-22 | 2025-01-08 | LG Chem, Ltd. | Method for preparing isopropyl alcohol |
| EP4549622A1 (en) | 2023-10-31 | 2025-05-07 | Basf Se | Hydrogenation of carbonyl compounds using hydrogen with low deuterium content |
| WO2025105774A1 (ko) * | 2023-11-15 | 2025-05-22 | 주식회사 엘지화학 | 이소프로필 알코올의 제조방법 |
| CN120641387A (zh) * | 2023-11-15 | 2025-09-12 | 株式会社Lg化学 | 纯化异丙醇的方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02174737A (ja) * | 1988-09-30 | 1990-07-06 | Mitsui Petrochem Ind Ltd | フェノールの製造方法およびその製造時の副生アセトンからプロピレンを得る方法 |
| WO2001062692A1 (en) * | 2000-02-25 | 2001-08-30 | Ineos Phenol Gmbh & Co. Kg | Process for preparing cumene which is used in the preparation of phenol |
| JP2002121160A (ja) * | 2000-10-16 | 2002-04-23 | Mitsui Chemicals Inc | イソプロピルアルコールの製造方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL59261C (cg-RX-API-DMAC7.html) | 1941-09-05 | |||
| JPS5550704B2 (cg-RX-API-DMAC7.html) * | 1972-06-08 | 1980-12-19 | ||
| US4480134A (en) * | 1983-04-05 | 1984-10-30 | General Electric Company | Process for preparing phenol and acetone from cumene |
| US5017729A (en) * | 1988-09-30 | 1991-05-21 | Mitsui Petrochemical Industries, Ltd. | Phenol preparation process and propylene recovery therefrom |
| CA2003925C (en) | 1988-11-28 | 1999-11-23 | Shintaro Araki | Preparation of cumene through alkylation of an aromatic compound and preparation of phenol through cumene |
| FR2656300B1 (fr) | 1989-12-21 | 1993-06-11 | Inst Francais Du Petrole | Procede de production de phenol. |
| KR100852565B1 (ko) * | 2000-09-25 | 2008-08-18 | 엑손모빌 케미칼 패턴츠 인코포레이티드 | 페놀 생산에서 분해 유출물의 수소화 방법 |
-
2002
- 2002-11-11 TW TW091133010A patent/TWI266762B/zh active
- 2002-11-12 CN CNB02822695XA patent/CN1266100C/zh not_active Ceased
- 2002-11-12 WO PCT/EP2002/012650 patent/WO2003011801A2/en not_active Ceased
- 2002-11-12 EP EP02779551A patent/EP1463700B1/en not_active Revoked
- 2002-11-12 AU AU2002342904A patent/AU2002342904A1/en not_active Abandoned
- 2002-11-12 AT AT02779551T patent/ATE361270T1/de not_active IP Right Cessation
- 2002-11-12 ES ES02779551T patent/ES2286298T3/es not_active Expired - Lifetime
- 2002-11-12 JP JP2003516996A patent/JP2004536147A/ja active Pending
- 2002-11-12 DE DE60219960T patent/DE60219960T2/de not_active Revoked
- 2002-11-12 KR KR10-2004-7007252A patent/KR20040055805A/ko not_active Ceased
- 2002-11-12 RU RU2004118066/04A patent/RU2296740C2/ru not_active IP Right Cessation
- 2002-11-12 BR BR0214170-1A patent/BR0214170A/pt not_active IP Right Cessation
- 2002-11-14 US US10/294,192 patent/US6939995B2/en not_active Expired - Fee Related
-
2004
- 2004-04-13 ZA ZA200402797A patent/ZA200402797B/en unknown
- 2004-05-13 MX MXPA04004553A patent/MXPA04004553A/es active IP Right Grant
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02174737A (ja) * | 1988-09-30 | 1990-07-06 | Mitsui Petrochem Ind Ltd | フェノールの製造方法およびその製造時の副生アセトンからプロピレンを得る方法 |
| WO2001062692A1 (en) * | 2000-02-25 | 2001-08-30 | Ineos Phenol Gmbh & Co. Kg | Process for preparing cumene which is used in the preparation of phenol |
| JP2002121160A (ja) * | 2000-10-16 | 2002-04-23 | Mitsui Chemicals Inc | イソプロピルアルコールの製造方法 |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007038217A (ja) * | 2005-07-30 | 2007-02-15 | Oxeno Olefinchemie Gmbh | 水素化触媒及びエステル含有アルデヒド混合物の接触水素化法 |
| WO2008062644A1 (fr) * | 2006-11-21 | 2008-05-29 | Mitsui Chemicals, Inc. | Procédé de fabrication d'un composé aromatique alkylé et procédé de fabrication de phénol |
| JPWO2008062644A1 (ja) * | 2006-11-21 | 2010-03-04 | 三井化学株式会社 | アルキル化芳香族化合物の製造方法およびフェノールの製造方法 |
| JP5296549B2 (ja) * | 2006-11-21 | 2013-09-25 | 三井化学株式会社 | アルキル化芳香族化合物の製造方法およびフェノールの製造方法 |
| US8581016B2 (en) | 2006-11-21 | 2013-11-12 | Mitsui Chemicals, Inc. | Process for producing alkylated aromatic compound and process for producing phenol |
| JP2008285477A (ja) * | 2007-04-18 | 2008-11-27 | Mitsui Chemicals Inc | アルキル化芳香族化合物の製造方法およびフェノールの製造方法 |
| WO2014002884A1 (ja) * | 2012-06-27 | 2014-01-03 | 三井化学株式会社 | イソプロパノールの製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| TW200407288A (en) | 2004-05-16 |
| RU2004118066A (ru) | 2006-01-10 |
| MXPA04004553A (es) | 2004-08-13 |
| BR0214170A (pt) | 2004-09-28 |
| DE60219960T2 (de) | 2008-01-17 |
| WO2003011801A3 (en) | 2004-02-19 |
| CN1585734A (zh) | 2005-02-23 |
| WO2003011801A2 (en) | 2003-02-13 |
| DE60219960D1 (de) | 2007-06-14 |
| EP1463700A2 (en) | 2004-10-06 |
| ES2286298T3 (es) | 2007-12-01 |
| KR20040055805A (ko) | 2004-06-26 |
| CN1266100C (zh) | 2006-07-26 |
| AU2002342904A1 (en) | 2003-02-17 |
| EP1463700B1 (en) | 2007-05-02 |
| ZA200402797B (en) | 2004-12-23 |
| US6939995B2 (en) | 2005-09-06 |
| TWI266762B (en) | 2006-11-21 |
| RU2296740C2 (ru) | 2007-04-10 |
| US20030149314A1 (en) | 2003-08-07 |
| ATE361270T1 (de) | 2007-05-15 |
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