JP2015536641A5 - - Google Patents
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- JP2015536641A5 JP2015536641A5 JP2015533235A JP2015533235A JP2015536641A5 JP 2015536641 A5 JP2015536641 A5 JP 2015536641A5 JP 2015533235 A JP2015533235 A JP 2015533235A JP 2015533235 A JP2015533235 A JP 2015533235A JP 2015536641 A5 JP2015536641 A5 JP 2015536641A5
- Authority
- JP
- Japan
- Prior art keywords
- ddg
- fdca
- derivative
- conversion
- acid
- 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.)
- Granted
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- 238000006243 chemical reaction Methods 0.000 claims description 88
- CHTHALBTIRVDBM-UHFFFAOYSA-N furan-2,5-dicarboxylic acid Chemical class OC(=O)C1=CC=C(C(O)=O)O1 CHTHALBTIRVDBM-UHFFFAOYSA-N 0.000 claims description 76
- 238000000034 method Methods 0.000 claims description 68
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 20
- 239000002253 acid Substances 0.000 claims description 18
- 150000007522 mineralic acids Chemical class 0.000 claims description 17
- 230000002194 synthesizing effect Effects 0.000 claims description 13
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 10
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 8
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 4
- 239000006184 cosolvent Substances 0.000 claims description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 4
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 230000000379 polymerizing effect Effects 0.000 claims description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 2
- 239000003208 petroleum Substances 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 239000012071 phase Substances 0.000 claims 2
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000012808 vapor phase Substances 0.000 claims 1
- IZSRJDGCGRAUAR-MROZADKFSA-M 5-dehydro-D-gluconate Chemical compound OCC(=O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O IZSRJDGCGRAUAR-MROZADKFSA-M 0.000 description 25
- PHOQVHQSTUBQQK-SQOUGZDYSA-N D-glucono-1,5-lactone Chemical compound OC[C@H]1OC(=O)[C@H](O)[C@@H](O)[C@@H]1O PHOQVHQSTUBQQK-SQOUGZDYSA-N 0.000 description 22
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 20
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 18
- RGHNJXZEOKUKBD-SQOUGZDYSA-N Gluconic acid Natural products OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 18
- 235000012208 gluconic acid Nutrition 0.000 description 18
- 239000000174 gluconic acid Substances 0.000 description 18
- 230000002255 enzymatic effect Effects 0.000 description 17
- AEMOLEFTQBMNLQ-UHFFFAOYSA-N beta-D-galactopyranuronic acid Natural products OC1OC(C(O)=O)C(O)C(O)C1O AEMOLEFTQBMNLQ-UHFFFAOYSA-N 0.000 description 16
- AEMOLEFTQBMNLQ-BZINKQHNSA-N D-Guluronic Acid Chemical compound OC1O[C@H](C(O)=O)[C@H](O)[C@@H](O)[C@H]1O AEMOLEFTQBMNLQ-BZINKQHNSA-N 0.000 description 14
- 239000000758 substrate Substances 0.000 description 12
- 239000008103 glucose Substances 0.000 description 10
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 10
- AEMOLEFTQBMNLQ-CLQWQSTFSA-N l-iduronic acid Chemical compound O[C@H]1O[C@H](C(O)=O)[C@H](O)[C@@H](O)[C@@H]1O AEMOLEFTQBMNLQ-CLQWQSTFSA-N 0.000 description 10
- KDOGLQUELUMIFG-UHFFFAOYSA-N 2,5-dioxohexanoic acid Chemical compound CC(=O)CCC(=O)C(O)=O KDOGLQUELUMIFG-UHFFFAOYSA-N 0.000 description 7
- XGGAWFDOIDZRPI-UHFFFAOYSA-N 4,6-Dihydroxy Natural products C1=C2OCOC2=CC(C2OC(C3C(OC(O)C32)C=2C=C3OCOC3=CC=2)O)=C1 XGGAWFDOIDZRPI-UHFFFAOYSA-N 0.000 description 7
- DSLZVSRJTYRBFB-LLEIAEIESA-N D-glucaric acid Chemical compound OC(=O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O DSLZVSRJTYRBFB-LLEIAEIESA-N 0.000 description 4
- 230000037361 pathway Effects 0.000 description 4
- QUURPCHWPQNNGL-ZAFYKAAXSA-N 5-dehydro-4-deoxy-D-glucaric acid Chemical group OC(=O)[C@H](O)[C@@H](O)CC(=O)C(O)=O QUURPCHWPQNNGL-ZAFYKAAXSA-N 0.000 description 3
- WTAHRPBPWHCMHW-PAKKCRSFSA-N 3-dehydro-D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)C(=O)[C@@H](O)C(O)=O WTAHRPBPWHCMHW-PAKKCRSFSA-N 0.000 description 2
- DSLZVSRJTYRBFB-LLEIAEIESA-L D-glucarate(2-) Chemical compound [O-]C(=O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O DSLZVSRJTYRBFB-LLEIAEIESA-L 0.000 description 2
- -1 guluronic acid lactone Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000009483 enzymatic pathway Effects 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261704408P | 2012-09-21 | 2012-09-21 | |
| US61/704,408 | 2012-09-21 | ||
| PCT/US2013/061036 WO2014047510A1 (en) | 2012-09-21 | 2013-09-20 | Compositions and methods for producing chemicals and derivatives thereof |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017091072A Division JP2017195885A (ja) | 2012-09-21 | 2017-05-01 | 化学物質およびその誘導体を生成するための組成物および方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015536641A JP2015536641A (ja) | 2015-12-24 |
| JP2015536641A5 true JP2015536641A5 (enExample) | 2016-10-27 |
| JP6163557B2 JP6163557B2 (ja) | 2017-07-12 |
Family
ID=50341985
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015533235A Expired - Fee Related JP6163557B2 (ja) | 2012-09-21 | 2013-09-20 | 化学物質およびその誘導体を生成するための組成物および方法 |
| JP2017091072A Pending JP2017195885A (ja) | 2012-09-21 | 2017-05-01 | 化学物質およびその誘導体を生成するための組成物および方法 |
| JP2018055638A Withdrawn JP2018139587A (ja) | 2012-09-21 | 2018-03-23 | 化学物質およびその誘導体を生成するための組成物および方法 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017091072A Pending JP2017195885A (ja) | 2012-09-21 | 2017-05-01 | 化学物質およびその誘導体を生成するための組成物および方法 |
| JP2018055638A Withdrawn JP2018139587A (ja) | 2012-09-21 | 2018-03-23 | 化学物質およびその誘導体を生成するための組成物および方法 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US9506090B2 (enExample) |
| EP (1) | EP2898083A4 (enExample) |
| JP (3) | JP6163557B2 (enExample) |
| CN (1) | CN104769122B (enExample) |
| AU (1) | AU2013317782B2 (enExample) |
| BR (1) | BR112015006255A2 (enExample) |
| CA (1) | CA2885662A1 (enExample) |
| SG (2) | SG10201702263QA (enExample) |
| WO (1) | WO2014047510A1 (enExample) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106414753A (zh) * | 2014-03-21 | 2017-02-15 | 合成基因组股份有限公司 | 用于生产化学品及其衍生物的组合物和方法 |
| WO2016057628A1 (en) * | 2014-10-09 | 2016-04-14 | Bp Corporation North America Inc. | Use of bromine ions in the production of 2,5-furandicarboxylic acid |
| CA2962622A1 (en) * | 2014-10-09 | 2016-04-14 | Bp Corporation North America Inc. | Use of halogens in the production of 2,5-furandicarboxylic acid |
| EP3204369A1 (en) * | 2014-10-09 | 2017-08-16 | BP Corporation North America Inc. | Use of an acidic solvent and water in the production of 2,5-furandicarboxylic acid |
| WO2016057682A1 (en) * | 2014-10-09 | 2016-04-14 | Bp Corporation North America Inc. | Use of reactants in the production of 2,5-furandicarboxylic acid |
| EP3204371A1 (en) * | 2014-10-09 | 2017-08-16 | BP Corporation North America Inc. | Use of carboxylic acids in the production of 2,5-furandicarboxylic acid |
| EP3778580B1 (en) * | 2015-03-05 | 2025-12-17 | BP Corporation North America Inc. | Synthesis of furans from sugars via keto intermediates |
| US10087161B2 (en) | 2015-08-20 | 2018-10-02 | Synthetic Genomics, Inc. | Synthesis of FDCA and FDCA precursors from gluconic acid derivatives |
| EP3402787A4 (en) | 2016-01-13 | 2019-11-27 | Stora Enso Oyj | PROCESS FOR THE PREPARATION OF 2,5-FURANDIC ACETIC ACID AND INTERMEDIATES AND DERIVATIVES THEREOF |
| US10927363B2 (en) | 2016-04-04 | 2021-02-23 | Mie University | DNA sequence and expression vector for alginate lyase |
| EP3458578A1 (en) * | 2016-05-20 | 2019-03-27 | Teknologian Tutkimuskeskus VTT OY | Improved meso-galactaric acid production from galacturonic acid with genetically modified fungal cells |
| CN107417651A (zh) * | 2017-06-20 | 2017-12-01 | 合肥利夫生物科技有限公司 | 一种制备2,5‑呋喃二甲酸及其衍生物的方法 |
| HUE061086T2 (hu) | 2017-06-22 | 2023-05-28 | Archer Daniels Midland Co | Eljárás furándikarbonsav-észterek elõállítására |
| SG11201913469PA (en) | 2017-07-12 | 2020-01-30 | Stora Enso Oyj | Purified 2,5-furandicarboxylic acid pathway products |
| EP3460067A1 (en) * | 2017-09-20 | 2019-03-27 | Technische Universität München | Process for enzymatic oxidation of linear carbohydrates |
| CN107954959A (zh) * | 2017-11-22 | 2018-04-24 | 南京工业大学 | 一种制备2,5-呋喃二甲酸及其前体物质的方法 |
| EP3963067A1 (en) * | 2019-07-11 | 2022-03-09 | BP Corporation North America Inc. | Gluconate dehydratase enzymes and recombinant cells |
| MX2022011053A (es) * | 2020-03-06 | 2023-03-14 | Solugen Inc | Composiciones y metodos para la obtencion de productos procedentes de la oxidacion de la glucosa. |
| US20230096662A1 (en) * | 2020-03-12 | 2023-03-30 | Solugen, Inc. | Compositions and methods for 2,5-furan dicarboxylic acid production |
| US12295919B2 (en) | 2022-03-16 | 2025-05-13 | Mie University | Methods of treatment and prevention using 4-deoxy-L-erythro-5-hexoseulose uronic acid |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3184479A (en) * | 1965-05-18 | Process for the preparation of | ||
| CH387656A (de) | 1961-03-07 | 1965-02-15 | Ciba Geigy | Verfahren zur Herstellung von 2,5-Furandicarbonsäure |
| US3203963A (en) | 1963-04-18 | 1965-08-31 | Atlas Chem Ind | Method of purifying dehydromucic acid |
| US3326944A (en) | 1964-03-09 | 1967-06-20 | Atlas Chem Ind | Method of producing dehydromucic acid |
| JP2850515B2 (ja) | 1990-09-25 | 1999-01-27 | 東洋紡績株式会社 | グルコースデヒドロゲナーゼおよびその製造法 |
| FR2723946B1 (fr) * | 1994-08-24 | 1996-10-18 | Ard Sa | Procede de fabrication d'un diester de l'acide 2,5-furane dicarboxylique |
| JP4804187B2 (ja) | 2006-03-28 | 2011-11-02 | キヤノン株式会社 | フラン−２，５−ジカルボン酸の製造方法 |
| JP5051509B2 (ja) * | 2006-11-16 | 2012-10-17 | 独立行政法人産業技術総合研究所 | ２，５−フランジカルボン酸ジエステルの製造方法 |
| EP2143785B1 (en) * | 2007-05-08 | 2011-10-12 | Ensuiko Sugar Refining Co., Ltd., | Method for producing glucuronic acid by glucuronic acid fermentation |
| US7385081B1 (en) | 2007-11-14 | 2008-06-10 | Bp Corporation North America Inc. | Terephthalic acid composition and process for the production thereof |
| SI2265709T1 (en) | 2008-03-27 | 2018-03-30 | Genomatica, Inc. | MICROORGANISMS FOR PREPARATION OF ADYPIC ACID AND OTHER COMPOUNDS |
| WO2009145838A2 (en) * | 2008-04-04 | 2009-12-03 | Massachusetts Institute Of Technology | Cellular production of glucaric acid |
| FI20086236A0 (fi) | 2008-12-23 | 2008-12-23 | Valtion Teknillinen | Heksuronihapon konversio heksarihapoksi |
| CA2775319C (en) | 2009-10-07 | 2018-08-28 | Furanix Technologies B.V. | Method for the preparation of 2,5-furandicarboxylic acid and for the preparation of the dialkyl ester of 2,5-furandicarboxylic acid |
| JP5550303B2 (ja) | 2009-10-19 | 2014-07-16 | キヤノン株式会社 | ２，５−フランジカルボン酸の製造方法 |
| WO2011081658A2 (en) | 2009-12-15 | 2011-07-07 | Qteros, Inc. | Methods and compositions for producing chemical products from c. phytofermentants |
| NL2006359C2 (en) | 2011-03-08 | 2012-04-24 | Bird Engineering B V | Genetically modified cell and process for use of said cell. |
| EP2503003A1 (en) | 2011-03-24 | 2012-09-26 | Volker Sieber | Synthetic pathway for the production of alcohols or amines |
| CN103492189B (zh) * | 2011-09-20 | 2015-09-16 | 尤尼卡技术股份有限公司 | 用于在包含彩色体的衬底上产生彩色图像的方法和设备以及由此制造的产品 |
| WO2013049711A1 (en) | 2011-09-29 | 2013-04-04 | Bio Architecture Lab, Inc. | Methods for preparing 2,5-furandicarboxylic acid |
| US9079844B2 (en) | 2012-04-04 | 2015-07-14 | Stichting Dienst Landbouwkundig Onderzoek | Catalytic oxidation of uronic acids to aldaric acids |
| CN105026548B (zh) * | 2012-06-04 | 2019-06-18 | 盐水港精糖株式会社 | D-葡萄糖二酸生产菌及d-葡萄糖二酸的制造方法 |
| US20150152452A1 (en) | 2012-07-20 | 2015-06-04 | Novozymes A/S | Enzymatic Oxidation of 5-Hydroxymethylfurfural and Derivatives Thereof |
-
2013
- 2013-09-20 BR BR112015006255A patent/BR112015006255A2/pt not_active Application Discontinuation
- 2013-09-20 SG SG10201702263QA patent/SG10201702263QA/en unknown
- 2013-09-20 WO PCT/US2013/061036 patent/WO2014047510A1/en not_active Ceased
- 2013-09-20 SG SG11201502143VA patent/SG11201502143VA/en unknown
- 2013-09-20 JP JP2015533235A patent/JP6163557B2/ja not_active Expired - Fee Related
- 2013-09-20 CN CN201380056638.0A patent/CN104769122B/zh not_active Expired - Fee Related
- 2013-09-20 US US14/033,300 patent/US9506090B2/en not_active Expired - Fee Related
- 2013-09-20 AU AU2013317782A patent/AU2013317782B2/en not_active Ceased
- 2013-09-20 CA CA2885662A patent/CA2885662A1/en not_active Abandoned
- 2013-09-20 EP EP13838235.3A patent/EP2898083A4/en not_active Withdrawn
-
2017
- 2017-05-01 JP JP2017091072A patent/JP2017195885A/ja active Pending
-
2018
- 2018-03-23 JP JP2018055638A patent/JP2018139587A/ja not_active Withdrawn
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