PL174067B1 - Sposób izomeryzacji kwasów karboksylowych - Google Patents
Sposób izomeryzacji kwasów karboksylowychInfo
- Publication number
- PL174067B1 PL174067B1 PL94310682A PL31068294A PL174067B1 PL 174067 B1 PL174067 B1 PL 174067B1 PL 94310682 A PL94310682 A PL 94310682A PL 31068294 A PL31068294 A PL 31068294A PL 174067 B1 PL174067 B1 PL 174067B1
- Authority
- PL
- Poland
- Prior art keywords
- acid
- reaction
- carried out
- amount
- promoter
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 48
- 150000001735 carboxylic acids Chemical class 0.000 title claims abstract description 18
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims abstract description 48
- 239000001361 adipic acid Substances 0.000 claims abstract description 24
- 235000011037 adipic acid Nutrition 0.000 claims abstract description 24
- 229910052741 iridium Inorganic materials 0.000 claims abstract description 13
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 13
- 239000003054 catalyst Substances 0.000 claims abstract description 11
- RVHOBHMAPRVOLO-UHFFFAOYSA-N 2-ethylbutanedioic acid Chemical class CCC(C(O)=O)CC(O)=O RVHOBHMAPRVOLO-UHFFFAOYSA-N 0.000 claims abstract description 5
- 238000010438 heat treatment Methods 0.000 claims abstract description 4
- WVUYYXUATWMVIT-UHFFFAOYSA-N 1-bromo-4-ethoxybenzene Chemical compound CCOC1=CC=C(Br)C=C1 WVUYYXUATWMVIT-UHFFFAOYSA-N 0.000 claims description 17
- 238000006243 chemical reaction Methods 0.000 claims description 16
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims description 14
- 239000011541 reaction mixture Substances 0.000 claims description 14
- 239000002904 solvent Substances 0.000 claims description 11
- 229910000043 hydrogen iodide Inorganic materials 0.000 claims description 9
- 238000006317 isomerization reaction Methods 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 8
- YIYBQIKDCADOSF-UHFFFAOYSA-N pentenoic acid group Chemical class C(C=CCC)(=O)O YIYBQIKDCADOSF-UHFFFAOYSA-N 0.000 claims description 8
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 claims description 8
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 7
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 7
- 229910000042 hydrogen bromide Inorganic materials 0.000 claims description 7
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical group I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- CUJRVFIICFDLGR-UHFFFAOYSA-N acetylacetonate Chemical compound CC(=O)[CH-]C(C)=O CUJRVFIICFDLGR-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 229940005605 valeric acid Drugs 0.000 claims description 4
- 229910052740 iodine Inorganic materials 0.000 claims description 3
- 239000011630 iodine Substances 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 150000002596 lactones Chemical class 0.000 claims description 2
- 239000007791 liquid phase Substances 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 239000012429 reaction media Substances 0.000 claims description 2
- -1 aromatic aliphatic carboxylic acids Chemical class 0.000 claims 1
- 229930195734 saturated hydrocarbon Natural products 0.000 claims 1
- 239000002253 acid Substances 0.000 abstract description 13
- 150000007513 acids Chemical class 0.000 abstract description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 13
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 7
- 229910052786 argon Inorganic materials 0.000 description 4
- GAEKPEKOJKCEMS-UHFFFAOYSA-N gamma-valerolactone Chemical compound CC1CCC(=O)O1 GAEKPEKOJKCEMS-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003708 ampul Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- XJMMNTGIMDZPMU-UHFFFAOYSA-N 3-methylglutaric acid Chemical compound OC(=O)CC(C)CC(O)=O XJMMNTGIMDZPMU-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 238000011141 high resolution liquid chromatography Methods 0.000 description 2
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000011877 solvent mixture Substances 0.000 description 2
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 1
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 description 1
- 239000004912 1,5-cyclooctadiene Substances 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- PQLVXDKIJBQVDF-UHFFFAOYSA-N acetic acid;hydrate Chemical compound O.CC(O)=O PQLVXDKIJBQVDF-UHFFFAOYSA-N 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 150000001351 alkyl iodides Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- JEGUKCSWCFPDGT-UHFFFAOYSA-N h2o hydrate Chemical compound O.O JEGUKCSWCFPDGT-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
- 229940102396 methyl bromide Drugs 0.000 description 1
- 239000003279 phenylacetic acid Substances 0.000 description 1
- 229960003424 phenylacetic acid Drugs 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000002994 raw material Substances 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
- 239000000243 solution Substances 0.000 description 1
- UIUWNILCHFBLEQ-NSCUHMNNSA-N trans-pent-3-enoic acid Chemical compound C\C=C\CC(O)=O UIUWNILCHFBLEQ-NSCUHMNNSA-N 0.000 description 1
- 230000009466 transformation Effects 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
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/353—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by isomerisation; by change of size of the carbon skeleton
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 (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9303703A FR2703045B1 (fr) | 1993-03-25 | 1993-03-25 | Procédé d'isomérisation d'acides carboxyliques. |
| PCT/FR1994/000247 WO1994021586A1 (fr) | 1993-03-25 | 1994-03-07 | Procede d'isomerisation d'acides carboxyliques |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL310682A1 PL310682A1 (en) | 1995-12-27 |
| PL174067B1 true PL174067B1 (pl) | 1998-06-30 |
Family
ID=9445530
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL94310682A PL174067B1 (pl) | 1993-03-25 | 1994-03-07 | Sposób izomeryzacji kwasów karboksylowych |
Country Status (16)
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5292944A (en) * | 1993-06-29 | 1994-03-08 | E. I. Du Pont De Nemours And Company | Process for the preparation of adipic acid or pentenoic acid |
| FR2749582B1 (fr) * | 1996-06-07 | 1998-07-17 | Rhone Poulenc Fibres | Procede d'hydroxycarbonylation des acides pentenoiques |
| EP3887596A4 (en) | 2018-11-29 | 2022-08-24 | RISE Innventia AB | Method of producing holocellulose and paper strength agent, process for the production of paper, the paper produced and use of the produced paper |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3090807A (en) * | 1958-07-31 | 1963-05-21 | Basf Ag | Isomerization of saturated aliphatic carboxylic acids |
| US3578688A (en) * | 1968-05-03 | 1971-05-11 | Union Oil Co | Isomerization of acids |
| US3592849A (en) * | 1969-01-21 | 1971-07-13 | Union Oil Co | Decomposition of anhydrides to isomeric acids |
| SU371198A1 (ru) * | 1971-04-19 | 1973-02-22 | Способ д//с-7яляс-изомеризации непредельных | |
| US4260820A (en) * | 1979-09-24 | 1981-04-07 | Texaco Development Corp. | Method of preparing aliphatic carboxylic acids |
| JPS6245854A (ja) * | 1985-11-25 | 1987-02-27 | 不二サッシ株式会社 | 太陽エネルギー収集屋根の下部接続部材 |
| DE3629512A1 (de) * | 1986-08-29 | 1988-03-03 | Huels Chemische Werke Ag | Verfahren zur isomerisierung unverzweigter funktionalisierter verbindungen mit endstaendigen doppelbindungen |
| US4939298A (en) * | 1988-12-12 | 1990-07-03 | E. I. Du Pont De Nemours And Company | Isomerization of carboxylic acids |
| JP6245854B2 (ja) | 2013-06-11 | 2017-12-13 | キヤノン株式会社 | 画像読取装置及びそれを備える画像形成装置 |
-
1993
- 1993-03-25 FR FR9303703A patent/FR2703045B1/fr not_active Expired - Fee Related
-
1994
- 1994-03-07 CN CN94191588A patent/CN1046264C/zh not_active Expired - Fee Related
- 1994-03-07 WO PCT/FR1994/000247 patent/WO1994021586A1/fr active IP Right Grant
- 1994-03-07 RU RU95122642A patent/RU2123490C1/ru not_active IP Right Cessation
- 1994-03-07 DE DE69412599T patent/DE69412599T2/de not_active Expired - Fee Related
- 1994-03-07 EP EP94909156A patent/EP0690836B1/fr not_active Expired - Lifetime
- 1994-03-07 SK SK1175-95A patent/SK281756B6/sk unknown
- 1994-03-07 CA CA002156418A patent/CA2156418A1/fr not_active Abandoned
- 1994-03-07 JP JP06520702A patent/JP3091493B2/ja not_active Expired - Fee Related
- 1994-03-07 PL PL94310682A patent/PL174067B1/pl not_active IP Right Cessation
- 1994-03-07 BR BR9406166A patent/BR9406166A/pt not_active IP Right Cessation
- 1994-03-07 SG SG1996003774A patent/SG74551A1/en unknown
- 1994-03-07 KR KR1019950704118A patent/KR100288999B1/ko not_active Expired - Fee Related
- 1994-03-07 CZ CZ19952441A patent/CZ287045B6/cs not_active IP Right Cessation
- 1994-03-30 TW TW083102739A patent/TW287155B/zh active
- 1994-07-03 UA UA95094230A patent/UA44242C2/uk unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2156418A1 (fr) | 1994-09-29 |
| CN1119855A (zh) | 1996-04-03 |
| EP0690836B1 (fr) | 1998-08-19 |
| BR9406166A (pt) | 1996-01-09 |
| KR960700990A (ko) | 1996-02-24 |
| DE69412599T2 (de) | 1999-05-27 |
| WO1994021586A1 (fr) | 1994-09-29 |
| DE69412599D1 (de) | 1998-09-24 |
| JP3091493B2 (ja) | 2000-09-25 |
| UA44242C2 (uk) | 2002-02-15 |
| EP0690836A1 (fr) | 1996-01-10 |
| TW287155B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1996-10-01 |
| JPH08506349A (ja) | 1996-07-09 |
| FR2703045B1 (fr) | 1995-05-19 |
| FR2703045A1 (fr) | 1994-09-30 |
| PL310682A1 (en) | 1995-12-27 |
| CZ287045B6 (en) | 2000-08-16 |
| SG74551A1 (en) | 2000-08-22 |
| RU2123490C1 (ru) | 1998-12-20 |
| CN1046264C (zh) | 1999-11-10 |
| SK281756B6 (sk) | 2001-07-10 |
| SK117595A3 (en) | 1996-04-03 |
| KR100288999B1 (ko) | 2001-05-02 |
| CZ244195A3 (en) | 1996-01-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Decisions on the lapse of the protection rights |
Effective date: 20060307 |