TW491834B - Process for the manufacture of quaternary carboxylic acids - Google Patents
Process for the manufacture of quaternary carboxylic acids Download PDFInfo
- Publication number
- TW491834B TW491834B TW088115042A TW88115042A TW491834B TW 491834 B TW491834 B TW 491834B TW 088115042 A TW088115042 A TW 088115042A TW 88115042 A TW88115042 A TW 88115042A TW 491834 B TW491834 B TW 491834B
- Authority
- TW
- Taiwan
- Prior art keywords
- acid
- scope
- item
- patent application
- weight
- Prior art date
Links
- 150000001735 carboxylic acids Chemical group 0.000 title claims abstract description 21
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 21
- 238000000034 method Methods 0.000 title claims abstract description 18
- 239000002253 acid Substances 0.000 claims abstract description 34
- 150000001336 alkenes Chemical class 0.000 claims abstract description 27
- 239000003054 catalyst Substances 0.000 claims abstract description 24
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims abstract description 18
- 238000006243 chemical reaction Methods 0.000 claims abstract description 17
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000002243 precursor Substances 0.000 claims abstract description 8
- 239000003960 organic solvent Substances 0.000 claims abstract description 6
- 239000011973 solid acid Substances 0.000 claims abstract description 5
- 150000002500 ions Chemical class 0.000 claims abstract description 4
- 230000002378 acidificating effect Effects 0.000 claims abstract description 3
- 239000002904 solvent Substances 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 13
- 239000011347 resin Substances 0.000 claims description 13
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 8
- 229920001577 copolymer Polymers 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 4
- -1 ethylene diene Chemical class 0.000 claims description 3
- 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 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- 239000003729 cation exchange resin Substances 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
- 229910014033 C-OH Inorganic materials 0.000 claims 1
- 229910014570 C—OH Inorganic materials 0.000 claims 1
- 101100289061 Drosophila melanogaster lili gene Proteins 0.000 claims 1
- JHGDVEYCZZGUIW-UHFFFAOYSA-N ethene styrene Chemical group C=C.C=C.C=CC1=CC=CC=C1 JHGDVEYCZZGUIW-UHFFFAOYSA-N 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 abstract description 2
- 229920001429 chelating resin Polymers 0.000 description 7
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- 229920000557 Nafion® Polymers 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- JYVLIDXNZAXMDK-UHFFFAOYSA-N pentan-2-ol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 229920005573 silicon-containing polymer Polymers 0.000 description 2
- 239000011949 solid catalyst Substances 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- CHRJZRDFSQHIFI-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;styrene Chemical compound C=CC1=CC=CC=C1.C=CC1=CC=CC=C1C=C CHRJZRDFSQHIFI-UHFFFAOYSA-N 0.000 description 1
- ZQXCQTAELHSNAT-UHFFFAOYSA-N 1-chloro-3-nitro-5-(trifluoromethyl)benzene Chemical compound [O-][N+](=O)C1=CC(Cl)=CC(C(F)(F)F)=C1 ZQXCQTAELHSNAT-UHFFFAOYSA-N 0.000 description 1
- OAOABCKPVCUNKO-UHFFFAOYSA-N 8-methyl Nonanoic acid Chemical compound CC(C)CCCCCCC(O)=O OAOABCKPVCUNKO-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003426 co-catalyst Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000002815 homogeneous catalyst Substances 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 230000003397 luteinic effect Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
- 230000037452 priming Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
- C07C51/12—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on an oxygen-containing group in organic compounds, e.g. alcohols
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
- C07C51/14—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on a carbon-to-carbon unsaturated bond in organic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP98203165 | 1998-09-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW491834B true TW491834B (en) | 2002-06-21 |
Family
ID=8234142
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW088115042A TW491834B (en) | 1998-09-21 | 1999-09-01 | Process for the manufacture of quaternary carboxylic acids |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP1115684B1 (enExample) |
| JP (1) | JP2002526464A (enExample) |
| KR (1) | KR100618260B1 (enExample) |
| CN (1) | CN1134396C (enExample) |
| AR (1) | AR020471A1 (enExample) |
| AU (1) | AU5980699A (enExample) |
| BR (1) | BR9913968A (enExample) |
| CA (1) | CA2344451C (enExample) |
| DE (1) | DE69904615T2 (enExample) |
| TW (1) | TW491834B (enExample) |
| WO (1) | WO2000017146A1 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2618778C (en) * | 2007-01-23 | 2016-04-05 | Linde, Inc. | Process for removing contaminants from gas streams |
| CN106631755A (zh) * | 2016-12-14 | 2017-05-10 | 安阳师范学院 | 强酸性离子交换树脂催化合成有机羧酸的方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS50123614A (enExample) * | 1974-03-15 | 1975-09-29 | ||
| JPS6176434A (ja) * | 1984-09-21 | 1986-04-18 | Idemitsu Petrochem Co Ltd | 第３級カルボン酸の製造方法 |
| JPS61118343A (ja) * | 1984-11-12 | 1986-06-05 | Agency Of Ind Science & Technol | カルボン酸及びカルボン酸誘導体の製造方法 |
| DE69512680T2 (de) * | 1994-12-28 | 2000-05-25 | Exxon Chemical Patents, Inc. | Herstellung von trialkylcarbonsäuren unter verwendung eines festen sauren harzkatalysatorsystems |
| WO1998038149A1 (en) * | 1997-02-25 | 1998-09-03 | Shell Internationale Research Maatschappij B.V. | Process for the manufacture of carboxylic acids |
| EP0968166B1 (en) * | 1997-02-25 | 2002-06-12 | Resolution Research Nederland B.V. | Process for the manufacture of carboxylic acids |
| JPH11315047A (ja) * | 1998-04-30 | 1999-11-16 | Agency Of Ind Science & Technol | 固体酸触媒による第三級カルボン酸の合成法 |
-
1999
- 1999-09-01 TW TW088115042A patent/TW491834B/zh not_active IP Right Cessation
- 1999-09-15 CA CA002344451A patent/CA2344451C/en not_active Expired - Fee Related
- 1999-09-15 CN CNB998111929A patent/CN1134396C/zh not_active Expired - Fee Related
- 1999-09-15 WO PCT/EP1999/006998 patent/WO2000017146A1/en not_active Ceased
- 1999-09-15 BR BR9913968-5A patent/BR9913968A/pt not_active Application Discontinuation
- 1999-09-15 EP EP99969406A patent/EP1115684B1/en not_active Expired - Lifetime
- 1999-09-15 JP JP2000574056A patent/JP2002526464A/ja active Pending
- 1999-09-15 AU AU59806/99A patent/AU5980699A/en not_active Abandoned
- 1999-09-15 DE DE69904615T patent/DE69904615T2/de not_active Expired - Lifetime
- 1999-09-15 KR KR1020017003447A patent/KR100618260B1/ko not_active Expired - Fee Related
- 1999-09-17 AR ARP990104675A patent/AR020471A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE69904615T2 (de) | 2004-07-01 |
| KR100618260B1 (ko) | 2006-09-01 |
| EP1115684A1 (en) | 2001-07-18 |
| CA2344451C (en) | 2009-04-07 |
| CN1134396C (zh) | 2004-01-14 |
| AR020471A1 (es) | 2002-05-15 |
| CA2344451A1 (en) | 2000-03-30 |
| EP1115684B1 (en) | 2002-12-18 |
| CN1319082A (zh) | 2001-10-24 |
| AU5980699A (en) | 2000-04-10 |
| BR9913968A (pt) | 2001-07-03 |
| JP2002526464A (ja) | 2002-08-20 |
| WO2000017146A1 (en) | 2000-03-30 |
| DE69904615D1 (de) | 2003-01-30 |
| KR20010075171A (ko) | 2001-08-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP1123264B1 (en) | Process for the manufacture of alpha,alpha-branched carboxylic acids | |
| TW491834B (en) | Process for the manufacture of quaternary carboxylic acids | |
| WO1981000846A1 (en) | The use of perfluorosulfonic acid resins as catalysts for preparing esters | |
| US5981796A (en) | Process for the manufacture of carboxylic acids | |
| EP0989969B1 (en) | Process for the manufacture of carboxylic acids | |
| EP0544790B1 (en) | Aquathermolytic cleavage of ethers | |
| JPH10511666A (ja) | 固体カチオン樹脂触媒系を用いるトリアルキル酢酸の製造 | |
| JP4025373B2 (ja) | カルボン酸の製造方法 | |
| WO2012017447A2 (en) | Method for selective hydration of aroma olefins to alcohols in continuous solid catalyst column reactor | |
| WO1998038149A1 (en) | Process for the manufacture of carboxylic acids | |
| EP3212607B1 (en) | Process for in situ water removal from an oxidative esterification reaction using a coupled reactor-distillation system | |
| EP3212606B1 (en) | Process for in situ water removal from an oxidative esterification reaction using a coupled reactor-distillation system | |
| WO2003024914A1 (en) | Manufacture of allyl esters of tertiary alkane carboxylic acids | |
| JP2001288144A (ja) | カルボニル化触媒及びギ酸エステルの製造方法 | |
| JP2000136164A (ja) | ジカルボン酸のジエステルの製造方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| GD4A | Issue of patent certificate for granted invention patent | ||
| MM4A | Annulment or lapse of patent due to non-payment of fees |