ATE222898T1 - Verfahren zur herstellung von gamma-butyrolacton und tetrahydrofuran - Google Patents
Verfahren zur herstellung von gamma-butyrolacton und tetrahydrofuranInfo
- Publication number
- ATE222898T1 ATE222898T1 AT99959273T AT99959273T ATE222898T1 AT E222898 T1 ATE222898 T1 AT E222898T1 AT 99959273 T AT99959273 T AT 99959273T AT 99959273 T AT99959273 T AT 99959273T AT E222898 T1 ATE222898 T1 AT E222898T1
- Authority
- AT
- Austria
- Prior art keywords
- maleic anhydride
- gamma butyrolactone
- mixture
- tetrahydrofuran
- butyrolactone
- Prior art date
Links
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 title abstract 16
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 title abstract 8
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 title abstract 4
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 6
- 239000000203 mixture Substances 0.000 abstract 5
- OYAKWDCOQQBJTJ-UHFFFAOYSA-N furan-2,5-dione;oxolan-2-one Chemical compound O=C1CCCO1.O=C1OC(=O)C=C1 OYAKWDCOQQBJTJ-UHFFFAOYSA-N 0.000 abstract 4
- 238000010521 absorption reaction Methods 0.000 abstract 3
- 239000007789 gas Substances 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 3
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 abstract 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 3
- 239000006096 absorbing agent Substances 0.000 abstract 2
- 238000005984 hydrogenation reaction Methods 0.000 abstract 2
- 230000003647 oxidation Effects 0.000 abstract 2
- 238000007254 oxidation reaction Methods 0.000 abstract 2
- 238000004064 recycling Methods 0.000 abstract 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000001273 butane Substances 0.000 abstract 1
- 239000006227 byproduct Substances 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 238000004821 distillation Methods 0.000 abstract 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 1
- 239000011976 maleic acid Substances 0.000 abstract 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 1
- 239000012808 vapor phase Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D307/30—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/32—Oxygen atoms
- C07D307/33—Oxygen atoms in position 2, the oxygen atom being in its keto or unsubstituted enol form
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D315/00—Heterocyclic compounds containing rings having one oxygen atom as the only ring hetero atom according to more than one of groups C07D303/00 - C07D313/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/06—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
- C07D307/08—Preparation of tetrahydrofuran
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE9800820A BE1012274A7 (fr) | 1998-11-10 | 1998-11-10 | Procede a haute productivite pour la preparation de gamma butyrolactone et de tetrahydrofurane. |
| PCT/EP1999/008536 WO2000027834A1 (en) | 1998-11-10 | 1999-11-08 | Process to afford gamma butyrolactone and tetrahydrofuran |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE222898T1 true ATE222898T1 (de) | 2002-09-15 |
Family
ID=3891519
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT99959273T ATE222898T1 (de) | 1998-11-10 | 1999-11-08 | Verfahren zur herstellung von gamma-butyrolacton und tetrahydrofuran |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US6433193B1 (de) |
| EP (1) | EP1129085B1 (de) |
| JP (1) | JP2002529459A (de) |
| KR (1) | KR100631251B1 (de) |
| CN (1) | CN1145620C (de) |
| AT (1) | ATE222898T1 (de) |
| AU (1) | AU1651300A (de) |
| BE (1) | BE1012274A7 (de) |
| DE (1) | DE69902683T2 (de) |
| ES (1) | ES2183630T3 (de) |
| WO (1) | WO2000027834A1 (de) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY139259A (en) * | 1999-10-12 | 2009-09-30 | Kvaerner Process Tech Ltd | Process |
| GB0325526D0 (en) | 2003-10-31 | 2003-12-03 | Davy Process Techn Ltd | Process |
| CN101868449B (zh) * | 2008-11-17 | 2014-10-01 | 巴斯夫欧洲公司 | 制备四氢呋喃的方法 |
| KR101241381B1 (ko) | 2010-02-24 | 2013-03-07 | 용산화학 주식회사 | 무수말레산의 제조방법 |
| CN102311332B (zh) * | 2010-07-07 | 2013-11-20 | 中国石油化工股份有限公司 | 一种生产丁二酸的方法 |
| EP2619193B1 (de) * | 2010-09-24 | 2014-11-12 | Basf Se | Verfahren zur gewinnung von tetrahydrofuran |
| EP2782893B1 (de) | 2011-11-25 | 2017-08-23 | Conser SPA | Verfahren zur herstellung von 1,4-butandiol, gamma-butyrolacton und tetrahydrofuran durch hydrierung von dialkylmaleat in einer gemischten flüssigkeits-/dampfphase |
| EP3288667A1 (de) * | 2015-04-30 | 2018-03-07 | Prosernat | Verfahren zur entfernung von aromatischen kohlenwasserstoffen aus der zufuhr von magerem sauergas zur schwefelwiedergewinnung |
| EP3559156A1 (de) * | 2016-12-20 | 2019-10-30 | SABIC Global Technologies B.V. | Verwendung eines normalkohlenstoff 4 (nc4)-recyclingstroms für sekundäre und tertiäre produkte |
| EP4188903B1 (de) | 2021-03-12 | 2024-01-03 | Conser S.P.A. | Verfahren zur gleichzeitigen herstellung von dialkylsuccinat und 1,4-butandiol durch hydrierung von dialkylmaleat in zwei stufen |
| CN115739111B (zh) * | 2022-11-17 | 2024-07-02 | 大连众智长兴精细化工有限公司 | 一种顺酐加氢制备丁二酸酐的催化剂及制备方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4609636A (en) | 1983-12-22 | 1986-09-02 | E. I. Du Pont De Nemours And Company | Pd/Re hydrogenation catalyst for making tetrahydrofuran and 1,4-butanediol |
| GB8707595D0 (en) * | 1987-03-31 | 1987-05-07 | British Petroleum Co Plc | Chemical process |
| GB2207914A (en) * | 1987-07-30 | 1989-02-15 | Davy Mckee | Process for the production of a mixture of butane 1,4-diol gamma-butyrolactone and tetrahydrofuran |
| US5149836A (en) | 1991-07-25 | 1992-09-22 | Isp Investments Inc. | Process for the production of gamma butyrolactone THF in predetermined amounts |
| US5478952A (en) | 1995-03-03 | 1995-12-26 | E. I. Du Pont De Nemours And Company | Ru,Re/carbon catalyst for hydrogenation in aqueous solution |
| ZA973972B (en) * | 1996-05-14 | 1998-03-23 | Kvaerner Process Tech Ltd | A process for the production of at least one C4 compound selected from butane-1,4-diol, gamma-butyrolactone and tetrahydrofuran. |
| ZA973971B (en) | 1996-05-15 | 1998-03-23 | Kvaerner Process Tech Ltd | A process for the production of at least one C4 compound selected from butane-1,4-diol, gamma-butyrolactone and tetrahydrofuran. |
-
1998
- 1998-11-10 BE BE9800820A patent/BE1012274A7/fr not_active IP Right Cessation
-
1999
- 1999-11-08 CN CNB998151610A patent/CN1145620C/zh not_active Expired - Fee Related
- 1999-11-08 KR KR1020017005915A patent/KR100631251B1/ko not_active Expired - Fee Related
- 1999-11-08 JP JP2000581012A patent/JP2002529459A/ja not_active Withdrawn
- 1999-11-08 EP EP99959273A patent/EP1129085B1/de not_active Expired - Lifetime
- 1999-11-08 AU AU16513/00A patent/AU1651300A/en not_active Abandoned
- 1999-11-08 WO PCT/EP1999/008536 patent/WO2000027834A1/en not_active Ceased
- 1999-11-08 US US09/831,403 patent/US6433193B1/en not_active Expired - Fee Related
- 1999-11-08 AT AT99959273T patent/ATE222898T1/de not_active IP Right Cessation
- 1999-11-08 DE DE69902683T patent/DE69902683T2/de not_active Expired - Fee Related
- 1999-11-08 ES ES99959273T patent/ES2183630T3/es not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| BE1012274A7 (fr) | 2000-08-01 |
| US6433193B1 (en) | 2002-08-13 |
| EP1129085B1 (de) | 2002-08-28 |
| EP1129085A1 (de) | 2001-09-05 |
| DE69902683T2 (de) | 2003-07-31 |
| CN1145620C (zh) | 2004-04-14 |
| WO2000027834A1 (en) | 2000-05-18 |
| DE69902683D1 (de) | 2002-10-02 |
| KR20010075697A (ko) | 2001-08-09 |
| JP2002529459A (ja) | 2002-09-10 |
| AU1651300A (en) | 2000-05-29 |
| CN1332735A (zh) | 2002-01-23 |
| ES2183630T3 (es) | 2003-03-16 |
| KR100631251B1 (ko) | 2006-10-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |