EA200600972A1 - Способ получения простых эфиров - Google Patents
Способ получения простых эфировInfo
- Publication number
- EA200600972A1 EA200600972A1 EA200600972A EA200600972A EA200600972A1 EA 200600972 A1 EA200600972 A1 EA 200600972A1 EA 200600972 A EA200600972 A EA 200600972A EA 200600972 A EA200600972 A EA 200600972A EA 200600972 A1 EA200600972 A1 EA 200600972A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- hydrogen
- stream
- zone
- anhydrides
- dicarboxylic acids
- Prior art date
Links
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
- C07D307/04—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)
Abstract
Способ получения простого эфира, необязательно вместе с диолом и/или лактоном, взаимодействием соответствующего органического исходного материала, выбранного из ненасыщенных дикарбоновых кислот и/или ангидридов, моноэфиров ненасыщенных дикарбоновых кислот и/или ангидридов, диэфиров ненасыщенных дикарбоновых кислот и/или ангидридов, ненасыщенных лактонов и смеси двух или более из этих компонентов в присутствии водорода, состоящий из следующих стадий: (а) подача потока, содержащего по меньшей мере часть органического исходного сырья в предреакторную зону, содержащую катализатор, и превращение в условиях реакции и контактирование указанного сырья с потоком, содержащим водород, происходящим таким образом, чтобы, по меньшей мере, некоторые из двойных углерод-углеродных связей стали насыщенными; (b) испарение, по меньшей мере, частично насыщенного сырья в поток, содержащий водород в зоне испарения; (с) подача потока, содержащего водород, содержащий, по меньшей мере, частично насыщенное сырье в парообразном состоянии, в реакционную зону, содержащую катализатор и функционирующую в условиях реакции; (d) отвод из реакционной зоны потока продукта, содержащего эфир и, необязательно, диол и/или лактон; и (е) возврат обедненного потока, содержащего водород, по меньшей мере, в предреакторную зону или зону испарения.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0329152.3A GB0329152D0 (en) | 2003-12-16 | 2003-12-16 | Process |
PCT/GB2004/005054 WO2005058855A1 (en) | 2003-12-16 | 2004-12-01 | Process for the production of ethers |
Publications (2)
Publication Number | Publication Date |
---|---|
EA200600972A1 true EA200600972A1 (ru) | 2006-10-27 |
EA010589B1 EA010589B1 (ru) | 2008-10-30 |
Family
ID=30471165
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200600972A EA010589B1 (ru) | 2003-12-16 | 2004-12-01 | Способ получения простых эфиров |
Country Status (20)
Country | Link |
---|---|
US (1) | US7598404B2 (ru) |
EP (1) | EP1694661B1 (ru) |
JP (1) | JP5013876B2 (ru) |
KR (1) | KR101144761B1 (ru) |
CN (1) | CN100577654C (ru) |
AR (1) | AR047147A1 (ru) |
AT (1) | ATE465155T1 (ru) |
AU (1) | AU2004299317B2 (ru) |
BR (1) | BRPI0417625B1 (ru) |
CA (1) | CA2548372C (ru) |
DE (1) | DE602004026773D1 (ru) |
EA (1) | EA010589B1 (ru) |
ES (1) | ES2344565T3 (ru) |
GB (1) | GB0329152D0 (ru) |
MX (1) | MXPA06006780A (ru) |
MY (1) | MY143519A (ru) |
NO (1) | NO20063214L (ru) |
TW (1) | TWI338005B (ru) |
WO (1) | WO2005058855A1 (ru) |
ZA (1) | ZA200605821B (ru) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0421928D0 (en) | 2004-10-01 | 2004-11-03 | Davy Process Techn Ltd | Process |
GB0803663D0 (en) * | 2008-02-28 | 2008-04-09 | Davy Process Techn Ltd | Process |
CN102190582B (zh) * | 2010-03-19 | 2014-06-18 | 上海焦化有限公司 | 一种同时生产丁二酸二甲酯和1,4-丁二醇的方法 |
US9186599B2 (en) | 2010-09-24 | 2015-11-17 | Basf Se | Process for isolating tetrahydrofuran |
CN103119033B (zh) | 2010-09-24 | 2015-12-02 | 巴斯夫欧洲公司 | 分离四氢呋喃的方法 |
CN102001939B (zh) * | 2010-10-26 | 2013-08-14 | 中国科学院山西煤炭化学研究所 | 一种丁二酸二羧酸酯的制备方法 |
CN103946201B (zh) | 2011-11-25 | 2017-03-08 | 康瑟公司 | 通过在混合的液相/气相中氢化马来酸二烷基酯生产1,4‑丁二醇的方法 |
US20130296585A1 (en) | 2012-03-30 | 2013-11-07 | Basf Corporation | Catalyst For Tetrahydrofuran Synthesis |
GB201318175D0 (en) | 2013-10-14 | 2013-11-27 | Johnson Matthey Davy Technologies Ltd | Process |
KR20220110820A (ko) | 2019-12-10 | 2022-08-09 | 바스프 에스이 | 중합체 침착물을 피하면서 1,4-부탄디올, 감마-부티로락톤 및 테트라하이드로푸란을 기상으로 제조하는 방법 |
EP4188903B1 (en) | 2021-03-12 | 2024-01-03 | Conser S.P.A. | Process for the co-production of dialkyl succinate and 1,4-butanediol by hydrogenating dialkyl maleate in two stages |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4830272A (ru) * | 1971-08-21 | 1973-04-21 | ||
JPS5318988B2 (ru) * | 1972-05-26 | 1978-06-17 | ||
DE2455617C3 (de) * | 1974-11-23 | 1982-03-18 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von Butandiol und/oder Tetrahydrofuran über die Zwischenstufe des γ-Butyrolactons |
BR8507068A (pt) * | 1984-11-21 | 1987-07-14 | Davy Mckee London | Processo para a producao de butano-1,4-diol |
US4626604A (en) * | 1985-09-11 | 1986-12-02 | Davy Mckee (London) Limited | Hydrogenation process |
BE1011699A6 (fr) * | 1998-01-08 | 1999-12-07 | Pantochim Sa | Procede de production de tetrahydrofuranne et de gamma-butyrolactone. |
BE1011698A6 (fr) * | 1998-01-08 | 1999-12-07 | Pantochim Sa | Procede de production de tetrahydrofuranne, de gamma-butyrolactone et de butanediol. |
EP1108702A1 (en) * | 1999-12-13 | 2001-06-20 | Kvaerner Process Technology Limited | Process for the co-production of aliphatic diols and cyclic ethers |
GB0117090D0 (en) * | 2001-07-12 | 2001-09-05 | Kvaerner Process Tech Ltd | Process |
-
2003
- 2003-12-16 GB GBGB0329152.3A patent/GB0329152D0/en not_active Ceased
-
2004
- 2004-11-26 TW TW093136631A patent/TWI338005B/zh not_active IP Right Cessation
- 2004-12-01 JP JP2006544534A patent/JP5013876B2/ja not_active Expired - Fee Related
- 2004-12-01 EP EP04801255A patent/EP1694661B1/en not_active Not-in-force
- 2004-12-01 WO PCT/GB2004/005054 patent/WO2005058855A1/en active Application Filing
- 2004-12-01 MX MXPA06006780A patent/MXPA06006780A/es active IP Right Grant
- 2004-12-01 ZA ZA200605821A patent/ZA200605821B/en unknown
- 2004-12-01 CN CN200480035623A patent/CN100577654C/zh active Active
- 2004-12-01 BR BRPI0417625-1B1A patent/BRPI0417625B1/pt not_active IP Right Cessation
- 2004-12-01 AT AT04801255T patent/ATE465155T1/de not_active IP Right Cessation
- 2004-12-01 KR KR1020067012060A patent/KR101144761B1/ko not_active IP Right Cessation
- 2004-12-01 EA EA200600972A patent/EA010589B1/ru not_active IP Right Cessation
- 2004-12-01 ES ES04801255T patent/ES2344565T3/es active Active
- 2004-12-01 CA CA2548372A patent/CA2548372C/en not_active Expired - Fee Related
- 2004-12-01 US US10/582,370 patent/US7598404B2/en not_active Expired - Fee Related
- 2004-12-01 DE DE602004026773T patent/DE602004026773D1/de active Active
- 2004-12-01 AU AU2004299317A patent/AU2004299317B2/en not_active Ceased
- 2004-12-03 MY MYPI20045021A patent/MY143519A/en unknown
- 2004-12-16 AR ARP040104689A patent/AR047147A1/es active IP Right Grant
-
2006
- 2006-07-11 NO NO20063214A patent/NO20063214L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
CN100577654C (zh) | 2010-01-06 |
DE602004026773D1 (de) | 2010-06-02 |
BRPI0417625A (pt) | 2007-03-27 |
MY143519A (en) | 2011-05-31 |
JP5013876B2 (ja) | 2012-08-29 |
AR047147A1 (es) | 2006-01-11 |
MXPA06006780A (es) | 2006-08-23 |
ZA200605821B (en) | 2008-05-28 |
KR101144761B1 (ko) | 2012-05-10 |
JP2007516978A (ja) | 2007-06-28 |
US7598404B2 (en) | 2009-10-06 |
NO20063214L (no) | 2006-07-11 |
ES2344565T3 (es) | 2010-08-31 |
EP1694661B1 (en) | 2010-04-21 |
CA2548372A1 (en) | 2005-06-30 |
EA010589B1 (ru) | 2008-10-30 |
GB0329152D0 (en) | 2004-01-21 |
AU2004299317B2 (en) | 2010-07-22 |
ATE465155T1 (de) | 2010-05-15 |
CN1890230A (zh) | 2007-01-03 |
WO2005058855A1 (en) | 2005-06-30 |
CA2548372C (en) | 2012-02-28 |
TW200535133A (en) | 2005-11-01 |
TWI338005B (en) | 2011-03-01 |
AU2004299317A1 (en) | 2005-06-30 |
US20070088169A1 (en) | 2007-04-19 |
BRPI0417625B1 (pt) | 2013-12-03 |
EP1694661A1 (en) | 2006-08-30 |
KR20060111584A (ko) | 2006-10-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
NO20063214L (no) | Fremgangsmate til fremstilling av etere | |
JP4990455B2 (ja) | トリグリセリドおよび脂肪酸の混合物から脂肪酸メチルエステルを生成する単相プロセス | |
Patel et al. | High conversion and productive catalyst turnovers in cross-metathesis reactions of natural oils with 2-butene | |
Malacea et al. | Renewable materials as precursors of linear nitrile-acid derivatives via cross-metathesis of fatty esters and acids with acrylonitrile and fumaronitrile | |
Rybak et al. | Cross-metathesis of fatty acid derivatives with methyl acrylate: renewable raw materials for the chemical industry | |
Nickel et al. | A highly efficient olefin metathesis process for the synthesis of terminal alkenes from fatty acid esters | |
BR9713206A (pt) | Método para produção de ésteres de ácidos graxos | |
EA200800292A1 (ru) | Способ получения пропиленгликоля | |
Pinto et al. | Hydrogenation of levulinic acid (LA) to γ-valerolactone (GVL) over Ni–Mo/C catalysts and water-soluble solvent systems | |
Sytniczuk et al. | Preparation of Musk‐Smelling Macrocyclic Lactones from Biomass: Looking for the Optimal Substrate Combination | |
Li et al. | Synthesis, isolation and characterization of methyl levulinate from cellulose catalyzed by extremely low concentration acid | |
Le Ravalec et al. | Improving Sustainability in Ene–Yne Cross‐Metathesis for Transformation of Unsaturated Fatty Esters | |
ES2052875T3 (es) | Procedimiento para preparar acido carboxilico insaturado o sus esteres. | |
EA200400173A1 (ru) | Способ получения простых эфиров, в типичном случае тетрагидрофурана | |
Le et al. | Efficient conversion of renewable unsaturated fatty acid methyl esters by cross-metathesis with eugenol | |
BRPI0513767A (pt) | método de co-produzir anidrido acético e um éster de acetato | |
ES2194356T3 (es) | Procedimiento para preparar gamma-butirolactona, butano-1,4-diol y tetrahidrofurano. | |
RU2494958C2 (ru) | Способ получения синтез-газа, ii | |
AR245686A1 (es) | Procedimiento para producir ester dimetilico del acido tereftalico a partir de p-xilol y metanol. | |
CN105308010B (zh) | 制备烯丙醇的方法以及由该方法制备的烯丙醇 | |
Li et al. | Palladium-catalyzed intermolecular alkynylcarbonylation of unactivated alkenes: easy access to β-alkynylcarboxylic esters | |
MY118197A (en) | Process for the preparation of butane-1,4-diol,gamma-butyrolactone and tetrahydrofuran | |
Mead et al. | A new approach to the preparation of 2-substituted tetrahydrofurans with alpha-syn selectivity | |
RU2008133565A (ru) | Катализатор для синтеза метанола, способ его получения и способ получения метанола | |
EA200600929A1 (ru) | Регулирование отношения этилена к пропилену, получаемых в процессе превращения кислородсодержащего вещества в олефины |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KZ KG MD TJ TM |
|
MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): RU |