JP2005500987A5 - - Google Patents

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Publication number
JP2005500987A5
JP2005500987A5 JP2002573769A JP2002573769A JP2005500987A5 JP 2005500987 A5 JP2005500987 A5 JP 2005500987A5 JP 2002573769 A JP2002573769 A JP 2002573769A JP 2002573769 A JP2002573769 A JP 2002573769A JP 2005500987 A5 JP2005500987 A5 JP 2005500987A5
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JP
Japan
Prior art keywords
metal catalyst
carried out
group
mpa
methylbutyrolactone
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.)
Withdrawn
Application number
JP2002573769A
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English (en)
Japanese (ja)
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JP2005500987A (ja
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Publication date
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Priority claimed from PCT/US2002/007878 external-priority patent/WO2002074760A1/en
Publication of JP2005500987A publication Critical patent/JP2005500987A/ja
Publication of JP2005500987A5 publication Critical patent/JP2005500987A5/ja
Withdrawn legal-status Critical Current

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JP2002573769A 2001-03-16 2002-03-14 レブリン酸からの5−メチルブチロラクトンの製造 Withdrawn JP2005500987A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US27658101P 2001-03-16 2001-03-16
PCT/US2002/007878 WO2002074760A1 (en) 2001-03-16 2002-03-14 Production of 5-methylbutyrolactone from levulinic acid

Publications (2)

Publication Number Publication Date
JP2005500987A JP2005500987A (ja) 2005-01-13
JP2005500987A5 true JP2005500987A5 (https=) 2005-06-09

Family

ID=23057217

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002573769A Withdrawn JP2005500987A (ja) 2001-03-16 2002-03-14 レブリン酸からの5−メチルブチロラクトンの製造

Country Status (8)

Country Link
US (1) US6617464B2 (https=)
EP (1) EP1368333A1 (https=)
JP (1) JP2005500987A (https=)
KR (1) KR20030082984A (https=)
CN (1) CN1498215A (https=)
BR (1) BR0208248A (https=)
CA (1) CA2437740A1 (https=)
WO (1) WO2002074760A1 (https=)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6946563B2 (en) * 2003-06-16 2005-09-20 E. I. Du Pont De Nemours And Company Production of 5-methyl-dihydro-furan-2-one from levulinic acid in supercritical media
US20060100449A1 (en) * 2004-11-10 2006-05-11 Manzer Leo E Integrated two-step process for the production of gamma-methyl-alpha-methylene-gamma-butyrolactone from levulinic acid and hydrogen
US20060100448A1 (en) * 2004-11-10 2006-05-11 Manzer Leo E Process for the production of Y-methyl-A-methylene-Y-butyrolactone from reaction of levulinic acid and hydrogen in the liquid phase followed by reaction of crude-Y-valerolactone and formaldehyde
US20060100447A1 (en) * 2004-11-10 2006-05-11 Manzer Leo E Process for the production of y-methyl-a-methylene-y-butyrolactone from reaction of levulinic acid and hydrogen with recycle of unreacted levulinic acid followed by reaction of crude y-valerolactone and formaldehyde, both reactions being carried out in the supercritical or near-critical fluid phase
US20060100450A1 (en) * 2004-11-10 2006-05-11 Manzer Leo E Process for the production of y-methyl-a-methylene-y-butyrolactone from reaction of levulinic acid and hydrogen followed by reaction of crude y-valerolactone and formaldehyde, both reactions being carried out in the supercritical or near-critical fluid phase
EP1828095B1 (en) 2004-12-23 2011-10-05 Shell Internationale Research Maatschappij B.V. A process for the hydrogenation of a lactone or of a carboxylic acid or an ester having a gamma-carbonyl group
CN101679183A (zh) * 2007-05-22 2010-03-24 国际壳牌研究有限公司 将乙酰丙酸转化为戊酸的方法
US20090069452A1 (en) * 2007-09-07 2009-03-12 Range Fuels, Inc Methods and apparatus for producing ethanol from syngas with high carbon efficiency
US7923405B2 (en) * 2007-09-07 2011-04-12 Range Fuels, Inc. Cobalt-molybdenum sulfide catalyst materials and methods for ethanol production from syngas
US20090156392A1 (en) * 2007-12-14 2009-06-18 Range Fuels, Inc. Catalyst compositions and methods for alcohol production from synthesis gas
US8354357B2 (en) * 2008-09-04 2013-01-15 Albemarle Corporation Cobalt-molybdenum sulfide catalyst materials and methods for stable alcohol production from syngas
US8586801B2 (en) 2008-09-04 2013-11-19 Albemarle Corporation Cobalt-molybdenum sulfide catalyst materials and methods for stable alcohol production from syngas
US8383691B2 (en) * 2009-06-30 2013-02-26 Albemarle Corporation Methods of making improved cobalt-molybdenum-sulfide catalyst compositions for higher alcohol synthesis
US8580978B2 (en) 2009-08-07 2013-11-12 Shell Oil Company Process for preparing a hydroxyacid or hydroxyester
US9012680B2 (en) 2009-08-07 2015-04-21 Shell Oil Company Process for preparing an ester
US20110112326A1 (en) * 2009-08-07 2011-05-12 Jean-Paul Lange Process for hydrogenation
EP2462100A1 (en) 2009-08-07 2012-06-13 Shell Internationale Research Maatschappij B.V. Process for hydrogenation
KR101231615B1 (ko) * 2009-09-11 2013-02-08 한국화학연구원 탄소수 4 내지 6의 유기산으로부터 고리화된 화합물을 제조하는 방법
CN101805316A (zh) * 2010-04-22 2010-08-18 复旦大学 一种用负载型铱催化剂制备γ-戊内酯的方法
PL2537840T3 (pl) 2011-06-21 2013-12-31 Dsm Ip Assets Bv Sposób wytwarzania walerolaktonu z kwasu lewulinowego
PL2573064T3 (pl) * 2011-09-23 2014-04-30 Dsm Ip Assets Bv Sposób wytwarzania estrów kwasu alkenowego z laktonów
CN102558108B (zh) * 2011-12-22 2014-07-16 南开大学 用铱-钳形配体络合物催化剂制备γ-戊内酯的方法
CN102617519B (zh) * 2012-03-05 2014-08-13 中国石油大学(华东) 由乙酰丙酸加氢制备γ-戊内酯的方法
EP2970166A4 (en) 2013-03-15 2016-11-23 Gfbiochemicals Ltd PROCESS FOR PRODUCING OCTANE DIOIC ACID, PRECURSORS AND DERIVATIVES
KR101333055B1 (ko) 2013-04-26 2013-11-27 박유성 발전기 및 그 제조방법
FR3008970B1 (fr) * 2013-07-25 2015-08-21 IFP Energies Nouvelles Procede de production d'alcools par hydrogenation catalytique d'acide levulinique en une etape
EP3204366B1 (en) 2014-10-08 2020-01-08 Council of Scientific and Industrial Research A process for the preparation of gamma-valerolactone by catalytic hydrogenation of levulinic acid using ru-based catalysts
CN104496945B (zh) * 2015-01-08 2016-06-22 山西大学 一种γ-戊内酯的制备方法
US10144718B2 (en) 2015-02-18 2018-12-04 Dsm Ip Assets B.V. Continuous hydrogenation of levulinic acid
WO2017061865A1 (en) 2015-10-06 2017-04-13 Avantium Knowledge Centre B.V. Process for the preparation of gamma-valerolactone
JP6558446B2 (ja) * 2015-11-16 2019-08-14 宇部興産株式会社 γ−バレロラクトンの製造方法
FI127020B (en) 2015-12-23 2017-09-29 Neste Oyj Selective method for the conversion of levulinic acid to gamma valerolactone
FI127191B (en) 2015-12-23 2018-01-15 Neste Oyj Combined production of levulinic acid and furfural from biomass
US9878967B2 (en) 2015-12-23 2018-01-30 Iowa State University Research Foundation, Inc. Method of converting levulinic acid or a derivative thereof to hydrocarbons and hydrogen, and methods of the production of hydrocarbons and hydrogen
CN108014798B (zh) * 2016-11-04 2020-10-30 中国石油化工股份有限公司 加氢制备2-甲基四氢呋喃的催化剂及其使用方法
CN109395723B (zh) * 2018-12-10 2021-08-31 郑州师范学院 一种乙酰丙酸加氢制γ-戊内酯Ru-Al催化体系及其制备方法和应用
CN110548505A (zh) * 2019-08-20 2019-12-10 青岛科技大学 核壳型催化剂及其合成方法、以及其催化乙酰丙酸制备γ-戊内酯的方法
SE546822C2 (en) * 2023-02-01 2025-02-25 Eco Oil Miljoebraenslen I Sverige Ab Process for continuous hydrogenation of aqueous levulinic acid to y-valerolactone and its tandem conversion to high octane gasoline range hydrocarbons

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2368366A (en) * 1942-08-21 1945-01-30 Monsanto Chemicals Process for the production of lactones
US2786852A (en) * 1953-08-19 1957-03-26 Quaker Oats Co Process of preparing gammavalerolactone
GB896949A (en) * 1957-12-14 1962-05-23 Basf Ag Improvements in the production of proto-anemonin and its homologues
NL8103173A (nl) * 1981-07-02 1983-02-01 Stamicarbon Werkwijze voor de bereiding van een 5-alkyl-butyrolacton.
US5883266A (en) * 1998-01-16 1999-03-16 Battelle Memorial Institute Hydrogenated 5-carbon compound and method of making

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