DE60315261D1 - Verfahren zur herstellung von 5-formyl-valeronsäurenitril unter verwendung eines reaktivierten katalysators - Google Patents

Verfahren zur herstellung von 5-formyl-valeronsäurenitril unter verwendung eines reaktivierten katalysators

Info

Publication number
DE60315261D1
DE60315261D1 DE60315261T DE60315261T DE60315261D1 DE 60315261 D1 DE60315261 D1 DE 60315261D1 DE 60315261 T DE60315261 T DE 60315261T DE 60315261 T DE60315261 T DE 60315261T DE 60315261 D1 DE60315261 D1 DE 60315261D1
Authority
DE
Germany
Prior art keywords
valeronic
formyl
preparation
acid
reactivated catalyst
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.)
Expired - Lifetime
Application number
DE60315261T
Other languages
English (en)
Other versions
DE60315261T2 (de
Inventor
Emilio Bunel
Marisa Bonilla
Ronnie Ozer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Invista Technologies SARL USA
Original Assignee
Invista Technologies SARL USA
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 Invista Technologies SARL USA filed Critical Invista Technologies SARL USA
Application granted granted Critical
Publication of DE60315261D1 publication Critical patent/DE60315261D1/de
Publication of DE60315261T2 publication Critical patent/DE60315261T2/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1845—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
    • B01J31/185—Phosphites ((RO)3P), their isomeric phosphonates (R(RO)2P=O) and RO-substitution derivatives thereof
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/40—Regeneration or reactivation
    • B01J31/4015—Regeneration or reactivation of catalysts containing metals
    • B01J31/4023—Regeneration or reactivation of catalysts containing metals containing iron group metals, noble metals or copper
    • B01J31/4038—Regeneration or reactivation of catalysts containing metals containing iron group metals, noble metals or copper containing noble metals
    • B01J31/4046—Regeneration or reactivation of catalysts containing metals containing iron group metals, noble metals or copper containing noble metals containing rhodium
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00—Preparation of carboxylic acid nitriles
    • C07C253/30—Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/32—Addition reactions to C=C or C-C triple bonds
    • B01J2231/321—Hydroformylation, metalformylation, carbonylation or hydroaminomethylation
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/822—Rhodium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1845—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/582—Recycling of unreacted starting or intermediate materials
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/584—Recycling of catalysts

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
DE60315261T 2002-03-12 2003-03-11 Verfahren zur herstellung von 5-formyl-valeronsäurenitril unter verwendung eines reaktivierten katalysators Expired - Lifetime DE60315261T2 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US10/096,781 US6750362B2 (en) 2002-03-12 2002-03-12 Process for making 5-formylvaleronitrile using reactivated catalyst
US96781 2002-03-12
PCT/US2003/007357 WO2003078385A1 (en) 2002-03-12 2003-03-11 Process for making 5-formylvaleronitrile using reactivated catalyst

Publications (2)

Publication Number Publication Date
DE60315261D1 true DE60315261D1 (de) 2007-09-13
DE60315261T2 DE60315261T2 (de) 2008-03-06

Family

ID=28039069

Family Applications (1)

Application Number Title Priority Date Filing Date
DE60315261T Expired - Lifetime DE60315261T2 (de) 2002-03-12 2003-03-11 Verfahren zur herstellung von 5-formyl-valeronsäurenitril unter verwendung eines reaktivierten katalysators

Country Status (11)

Country Link
US (1) US6750362B2 (de)
EP (1) EP1483234B1 (de)
JP (1) JP2005519967A (de)
CN (1) CN1326833C (de)
AT (1) ATE368642T1 (de)
AU (1) AU2003220150A1 (de)
DE (1) DE60315261T2 (de)
ES (1) ES2290445T3 (de)
MY (1) MY128519A (de)
TW (1) TWI257879B (de)
WO (1) WO2003078385A1 (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102909055B (zh) * 2011-08-01 2015-04-15 中国石油化工股份有限公司 金属磷化物型加氢裂化催化剂的制备方法
CN102909053B (zh) * 2011-08-01 2014-12-31 中国石油化工股份有限公司 中油型加氢裂化催化剂的制备方法
CN102909056B (zh) * 2011-08-01 2015-02-18 中国石油化工股份有限公司 含金属磷化物中油型加氢裂化催化剂的制备方法
KR101429808B1 (ko) * 2012-05-25 2014-08-18 주식회사 엘지화학 수소화 촉매의 재생방법
US9492813B2 (en) 2012-05-25 2016-11-15 Lg Chem, Ltd. Method for regenerating hydrogenation catalyst
EP3318570B1 (de) 2016-11-08 2019-08-07 Evonik Degussa GmbH Phosphorigsäure-p,p'-[5,5',6,6'-tetramethyl-3,3'-bis(1-methylethyl)[1,1'-biphenyl]-2,2'-diyl] p,p,p',p'-tetrakis(2,4-dimethylphenyl)-ester in der hydroformylierung

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04225841A (ja) * 1990-12-27 1992-08-14 Mitsubishi Kasei Corp ヒドロホルミル化触媒の賦活法
US5986126A (en) 1999-01-25 1999-11-16 E. I. Du Pont De Nemours And Company Process for the production of 6-aminocapronitrile and/or hexamethylenediamine
US6515161B1 (en) * 1999-09-20 2003-02-04 E. I. Du Pont De Nemours And Company Hydroformylation process utilizing multidentate phosphite ligands
US6307107B1 (en) * 1999-09-20 2001-10-23 E.I. Du Pont De Nemours And Company Hydroformylation of acyclic monoethylenically unsaturated compounds to corresponding terminal aldehydes
US6372939B1 (en) * 2000-11-16 2002-04-16 E.I. Du Pont De Nemours And Company Production of 6-aminocaproic acid

Also Published As

Publication number Publication date
CN1326833C (zh) 2007-07-18
MY128519A (en) 2007-02-28
US6750362B2 (en) 2004-06-15
DE60315261T2 (de) 2008-03-06
CN1653038A (zh) 2005-08-10
ATE368642T1 (de) 2007-08-15
AU2003220150A1 (en) 2003-09-29
TW200303786A (en) 2003-09-16
US20030176720A1 (en) 2003-09-18
EP1483234B1 (de) 2007-08-01
WO2003078385A1 (en) 2003-09-25
ES2290445T3 (es) 2008-02-16
TWI257879B (en) 2006-07-11
EP1483234A1 (de) 2004-12-08
JP2005519967A (ja) 2005-07-07

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