[go: up one dir, main page]

DK1556320T3 - Fremgangsmåde til fremstilling af 1,3-propandiol - Google Patents

Fremgangsmåde til fremstilling af 1,3-propandiol Download PDF

Info

Publication number
DK1556320T3
DK1556320T3 DK03779422.9T DK03779422T DK1556320T3 DK 1556320 T3 DK1556320 T3 DK 1556320T3 DK 03779422 T DK03779422 T DK 03779422T DK 1556320 T3 DK1556320 T3 DK 1556320T3
Authority
DK
Denmark
Prior art keywords
ruthenium
catalyst
metal
hydroxypropionic acid
group
Prior art date
Application number
DK03779422.9T
Other languages
English (en)
Inventor
Xiangsheng Meng
Timothy Abraham
Paris Tsobanakis
Original Assignee
Novozymes As
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Novozymes As filed Critical Novozymes As
Application granted granted Critical
Publication of DK1556320T3 publication Critical patent/DK1556320T3/da

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/147Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
    • C07C29/149Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof with hydrogen or hydrogen-containing gases
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12CBEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
    • C12C11/00Fermentation processes for beer
    • C12C11/02Pitching yeast

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Mycology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Microbiology (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Claims (22)

1
1. Fremgangsmåde til fremstilling af 1,3-propandiol omfattende at hydrere 3-hydroxypropionsyre i en væskefase, i tilstedeværelsen af en katalysator 5 omfattende ruthenium.
2. Fremgangsmåde ifølge krav 1 hvor væskefasen vælges fra gruppen bestående afvand, organisk opløsningsmiddel som ikke er hydrogenerbart, og en blanding af vand og det organiske opløsningsmiddel. 10
3. Fremgangsmåde ifølge krav 1, hvor katalysatoren omfattende ruthenium vælges fra gruppen bestående af rutheniummetal og forbindelser af rutheniummetal.
4. Fremgangsmåde ifølge krav 1 hvor rutheniumkatalysatoren omfatter en støttet rutheniumkatalysator.
5. Fremgangsmåde ifølge krav 4, hvor den støttede rutheniumkatalysator omfatter ruthenium på en kulstofstøtte. 20
6. Fremgangsmåde ifølge krav 1, hvor temperaturen er fra omkring 20°C til omkring 250°C.
7. Fremgangsmåde ifølge krav 1, hvor trykket er fra omkring 137895 Pa til 25 omkring 27579029 Pa.
8. Fremgangsmåde til fremstilling af 1,3-propandiol omfattende at hydrere 3-hydroxypropionsyre eller en C1-C20 alkylester deraf i en væskefase, i tilstedeværelsen af en katalysator omfattende, i kombination, en 30 rutheniumkatalysator og mindst en eller flere yderligere metalkatalysator(er) hvor det yderligere metal er valgt fra gruppen bestående af molybdæn, tungsten, titanium, zirkonium, niobium, vanadium, krom, og blandinger deraf.
9. Fremgangsmåde ifølge krav 8, hvor forbindelsen er 3-hydroxypropionsyre. 35 2
10. Fremgangsmåde ifølge krav 8, hvor forbindelsen er en C1-C5 ester af 3-hydroxypropionsyre.
11. Fremgangsmåde ifølge krav 8, hvor væskefasen vælges fra gruppen 5 bestående afvand, organisk opløsningsmiddel som ikke er hydrogenerbart, og en blanding af vand og det organiske opløsningsmiddel.
12. Fremgangsmåde ifølge krav 8, hvor rutheniumkatalysatoren vælges fra gruppen bestående af rutheniummetal og forbindelser af rutheniummetal. 10
13. Fremgangsmåde ifølge krav 8, hvor rutheniumkatalysatoren omfatter en støttet rutheniumkatalysator.
14. Fremgangsmåde ifølge krav 13, hvor den støttede rutheniumkatalysator 15 omfatter ruthenium på en kulstofstøtte.
15. Fremgangsmåde ifølge krav 8, hvor den yderligere metalkatalysator omfatter et metal eller en forbindelse af metallet, hvor metallet vælges fra gruppen bestående af molybdæn, tungsten, titanium, zirkonium, niobium, vanadium, 20 krom, og blandinger deraf.
16. Fremgangsmåde ifølge krav 15, hvor metallet er molybdæn.
17. Fremgangsmåde ifølge krav 8, hvor den yderligere metalkatalysator omfatter 25 en støttet metalkatalysator.
18. Fremgangsmåde ifølge krav 8, hvor temperaturen er fra omkring 20°C til omkring 250°C.
19. Fremgangsmåde ifølge krav 8, hvor trykket er fra omkring 137895 Pa til omkring 27579029 Pa.
20. Fremgangsmåde ifølge krav 8, hvor katalysatoren omfatter ruthenium på en kulstofstøtte og en yderligere metalkatalysator valgt fra gruppen bestående af 35 molybdæn og en molybdænoxid. 3
21. Fremgangsmåde ifølge krav 20, hvor forbindelsen er 3-hydroxypropionsyre.
22. Fremgangsmåde ifølge krav 1 eller 8, hvor 3-hydroxypropionsyren fremstilles fra en gensplejset organisme. 5
DK03779422.9T 2002-11-01 2003-10-30 Fremgangsmåde til fremstilling af 1,3-propandiol DK1556320T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US42306802P 2002-11-01 2002-11-01
PCT/US2003/034470 WO2004041421A2 (en) 2002-11-01 2003-10-30 Process for preparation of 1,3-propanediol

Publications (1)

Publication Number Publication Date
DK1556320T3 true DK1556320T3 (da) 2015-06-08

Family

ID=32312597

Family Applications (1)

Application Number Title Priority Date Filing Date
DK03779422.9T DK1556320T3 (da) 2002-11-01 2003-10-30 Fremgangsmåde til fremstilling af 1,3-propandiol

Country Status (10)

Country Link
US (1) US7126034B2 (da)
EP (1) EP1556320B1 (da)
JP (1) JP2006504788A (da)
CN (1) CN100381411C (da)
AU (1) AU2003285106A1 (da)
BR (1) BR0315969B1 (da)
CA (1) CA2503967A1 (da)
DK (1) DK1556320T3 (da)
MX (1) MXPA05004561A (da)
WO (1) WO2004041421A2 (da)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2008012560A (es) * 2006-10-27 2008-10-14 Archer Daniels Midland Co Procesos para aislar o purificar propilenglicol, etilenglicol y productos producidos de los mismos.
US8048624B1 (en) 2007-12-04 2011-11-01 Opx Biotechnologies, Inc. Compositions and methods for 3-hydroxypropionate bio-production from biomass
WO2010079500A2 (en) 2008-02-28 2010-07-15 Reliance Life Sciences Pvt. Ltd Aerobic production of 1,3-propanediol from crude glycerol from biodiesel process.
US8809027B1 (en) 2009-09-27 2014-08-19 Opx Biotechnologies, Inc. Genetically modified organisms for increased microbial production of 3-hydroxypropionic acid involving an oxaloacetate alpha-decarboxylase
JP2013505727A (ja) 2009-09-27 2013-02-21 オーピーエックス バイオテクノロジーズ, インコーポレイテッド 3−ヒドロキシプロピオン酸および他の生成物を生成するための方法
US9090918B2 (en) 2010-11-22 2015-07-28 Novozymes A/A Compositions and methods for 3-hydroxypropionic acid production
EP3385388A1 (en) 2011-03-22 2018-10-10 OPX Biotechnologies Inc. Microbial production of chemical products and related compositions, methods and systems
JP5878313B2 (ja) * 2011-07-22 2016-03-08 株式会社日本触媒 3−ヒドロキシプロピオン酸溶液の取扱い方法または保管の方法
US20140051136A1 (en) 2012-08-10 2014-02-20 Opx Biotechnologies, Inc. Micoorganisms and Methods for the Production of Fatty Acids and Fatty Acid Derived Products
US9108895B2 (en) 2012-10-26 2015-08-18 Eastman Chemical Company Promoted ruthenium catalyst for the improved hydrogenation of carboxylic acids to the corresponding alcohols
PL2970086T3 (pl) 2013-03-15 2019-04-30 Cargill Inc Odzyskiwanie kwasu 3-hydroksypropionowego
US20150119601A1 (en) 2013-03-15 2015-04-30 Opx Biotechnologies, Inc. Monofunctional mcr + 3-hp dehydrogenase
US9512057B2 (en) 2013-03-15 2016-12-06 Cargill, Incorporated 3-hydroxypropionic acid compositions
CN104117354A (zh) * 2013-04-26 2014-10-29 中国科学院大连化学物理研究所 有机酸水相低温选择性加氢制备一元醇或二元醇的方法
JP6603658B2 (ja) 2013-07-19 2019-11-06 カーギル インコーポレイテッド 脂肪酸及び脂肪酸誘導体の製造のための微生物及び方法
US11408013B2 (en) 2013-07-19 2022-08-09 Cargill, Incorporated Microorganisms and methods for the production of fatty acids and fatty acid derived products
EP2993228B1 (en) 2014-09-02 2019-10-09 Cargill, Incorporated Production of fatty acid esters
EP3577227A4 (en) 2017-02-02 2020-12-30 Cargill Inc. GENETICALLY MODIFIED CELLS PRODUCING C6-C10 FATTY ACID DERIVATIVES
KR102287646B1 (ko) * 2018-12-31 2021-08-06 한화솔루션 주식회사 탄소 기반의 귀금속-전이금속 복합촉매 및 이의 제조방법

Family Cites Families (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2094611A (en) 1934-12-11 1937-10-05 Du Pont Process for producing alcohols from hydroxy carboxylic compounds
US3770837A (en) * 1971-01-05 1973-11-06 Celanese Corp Hydrogenolysis of beta hydroxy carboxylic acid lactones
US4326072A (en) 1980-07-01 1982-04-20 Ici Americas Inc. Ruthenium catalyzed hydrogenation of D-glucuronic acid
GB8310797D0 (en) 1983-04-21 1983-05-25 British Petroleum Co Plc Vapour phase hydrogenation of esters
GB8509530D0 (en) 1985-04-13 1985-05-15 Bp Chem Int Ltd Hydrogenation of carboxylic acids
JPH064544B2 (ja) 1987-06-19 1994-01-19 高砂香料工業株式会社 光学活性アルコ−ルの製造方法
JP3381804B2 (ja) 1993-07-27 2003-03-04 荒川化学工業株式会社 カルボン酸直接還元用触媒および該触媒の製造方法ならびにアルコール化合物の製造方法
GB9324823D0 (en) 1993-12-02 1994-01-19 Davy Mckee London Process
GB9324786D0 (en) 1993-12-02 1994-01-19 Davy Mckee London Process
WO1995024371A1 (fr) * 1994-03-09 1995-09-14 Sagami Chemical Research Center Procede de production d'alcool
DE4444109A1 (de) * 1994-12-12 1996-06-13 Bayer Ag Verfahren zur Herstellung von optisch aktiven Alkoholen
US5686276A (en) 1995-05-12 1997-11-11 E. I. Du Pont De Nemours And Company Bioconversion of a fermentable carbon source to 1,3-propanediol by a single microorganism
JP3857360B2 (ja) * 1995-09-05 2006-12-13 財団法人相模中央化学研究所 ジオールの製造方法
US5698749A (en) 1995-09-06 1997-12-16 The Standard Oil Company Catalysts for the hydrogenation of aqueous maleic acid to 1,4-butanediol
MY118128A (en) 1996-03-01 2004-09-30 Basf Ag The preparation of 1, 6-hexanediol and caprolactone
JPH09241192A (ja) * 1996-03-08 1997-09-16 Sagami Chem Res Center アルコール類の製造方法
US5786524A (en) * 1996-05-30 1998-07-28 Shell Oil Company Process for preparation of 1,3-propanediol via hydrogenation of 3-hydroxypropanal
JP3887845B2 (ja) 1996-06-28 2007-02-28 三菱化学株式会社 水素化反応用触媒、その製造法、及び該触媒を用いた水素化反応方法
US6005137A (en) 1997-06-10 1999-12-21 3M Innovative Properties Company Halogenated acrylates and polymers derived therefrom
JP3979702B2 (ja) 1997-06-11 2007-09-19 イノヴィーン ユーエスエイ エルエルシー 水性マレイン酸を水素化して1,4−ブタンジオールとするための改善された触媒
DE69817356T2 (de) * 1997-06-18 2004-07-08 E.I. Du Pont De Nemours And Co., Wilmington Verfahren zur herstellung von 1,3-propandiol durch hydrierung von 3-hydroxypropanal
DE19803888A1 (de) 1998-01-31 1999-08-05 Bayer Ag Verfahren zur Herstellung von Ruthenium enthaltenden Katalysatoren und deren Verwendung bei Hydrierungen
DE19803893A1 (de) * 1998-01-31 1999-08-05 Bayer Ag Verfahren zur Herstellung von optisch aktiven Alkoholen
US6191321B1 (en) 1998-09-30 2001-02-20 Shell Oil Company Process for preparing 1,3-propanediol from methyl 3-hydroxypropionate
US6403844B1 (en) * 1998-11-24 2002-06-11 Board Of Trustees Of Michigan State University Condensed phase catalytic hydrogenation of lactic acid to propylene glycol
JP4282832B2 (ja) 1999-06-17 2009-06-24 旭化成ケミカルズ株式会社 ジオール類の製造法
JP4282830B2 (ja) 1999-06-17 2009-06-24 旭化成ケミカルズ株式会社 ジオール類の製造方法
JP4282831B2 (ja) 1999-06-17 2009-06-24 旭化成ケミカルズ株式会社 ジオール類の製法
US6455742B1 (en) 1999-09-02 2002-09-24 Wisconsin Alumni Research Foundation Method for catalytically reducing carboxylic acid groups to hydroxyl groups in hydroxycarboxylic acids
JP4472109B2 (ja) * 1999-09-21 2010-06-02 旭化成ケミカルズ株式会社 カルボン酸水添用触媒
JP4472108B2 (ja) * 1999-09-21 2010-06-02 旭化成ケミカルズ株式会社 カルボン酸水添触媒
GB2362157A (en) 2000-03-20 2001-11-14 Kvaerner Process Tech Ltd Preparation of Propane-1,3-Diol
DE10054347A1 (de) * 2000-11-02 2002-05-08 Degussa Verfahren zur katalytischen Hydrierung organischer Verbindungen und Trägerkatalysatoren hierfür
AU2002219818B2 (en) * 2000-11-20 2007-08-16 Cargill, Incorporated 3-hydroxypropionic acid and other organic compounds
EP1211234A3 (en) * 2000-11-29 2003-11-26 Samsung Electronics Co., Ltd. Process for preparing 1,3-alkandiols from 3-hydroxyesters
US6617478B2 (en) * 2000-11-29 2003-09-09 Samsung Electronics Co., Ltd. Process for preparing a 1,3-alkandiol from 3-hydroxyester

Also Published As

Publication number Publication date
AU2003285106A1 (en) 2004-06-07
JP2006504788A (ja) 2006-02-09
MXPA05004561A (es) 2005-07-26
BR0315969B1 (pt) 2013-03-19
US20050283029A1 (en) 2005-12-22
CA2503967A1 (en) 2004-05-21
US7126034B2 (en) 2006-10-24
EP1556320A2 (en) 2005-07-27
EP1556320B1 (en) 2015-05-13
CN100381411C (zh) 2008-04-16
WO2004041421A3 (en) 2004-06-10
EP1556320A4 (en) 2006-06-21
CN1711228A (zh) 2005-12-21
BR0315969A (pt) 2005-09-20
WO2004041421A2 (en) 2004-05-21

Similar Documents

Publication Publication Date Title
DK1556320T3 (da) Fremgangsmåde til fremstilling af 1,3-propandiol
CA2100229C (en) Process for the preparation of 1,3-propanediol
EP0524713B1 (en) Method for the manufacture of 1,3-Propanediol
EP0601571A1 (en) Method for purifying 1,4-butanediol, by hydrogenation and distillation
US20120010419A1 (en) Method for producing 1,6-hexanediol and caprolactone
ZA200607633B (en) Process for production of purified alcohols
EP0653406B1 (en) Use of supported rhodium catalysts in the preparation of tertiary butyl alcohol from tertiary butyl hydroperoxide
US9475786B2 (en) Method for synthesising 2,5-di(hydroxymethyl)furan and 2,5-di(hydroxymethyl)tetrahydrofuran by selective hydrogenation of furan-2,5-dialdehyde
US7329785B2 (en) Process for the production of 1,3-propanediol by catalytic hydrogenation of 3-hydroxypropanal in the presence of a hydration co-catalyst
US9975827B2 (en) Method for manufacturing 2,3-butanediol
KR100529763B1 (ko) 벤젠디메탄올 화합물의 제조방법
DE69404951T2 (de) Verwendung von Titania oder Zirconia zur Herstellung von Tertiärbutylalkohol aus Tertiärbutylhydroperoxid
US11247956B2 (en) Catalytic production of 1,2,5,6-hexanetetrol from levoglucosenone
JP4200704B2 (ja) フッ素化ベンゾニトリルの製造方法
EP0653404B1 (en) Use of supported chromium catalyst in the preparation of tertiary butyl alcohol from tertiary butyl hydroperoxide
JPH07196555A (ja) tert−ブチルヒドロペルオキシドの接触分解によるtert−ブチルアルコールの製造方法
EP0653402B1 (en) Use of supported lead oxide catalyst in the preparation of tertiary butyl alcohol from tertiary butyl hydroperoxide
US5471003A (en) Purification of cyclopropanecarboxaldehyde
JP2005247840A (ja) 1,3−プロパンジオールの製造方法及び該製造方法で得られる1,3−プロパンジオール
EP0653405B1 (en) Use of supported palladium/platinum catalysts in the preparation of tertiary butyl alcohol from tertiary butyl hydroperoxide