PL3319951T3 - Sposób hydroformylowania 2-podstawionych butadienów oraz wytwarzania ich produktów pochodnych, w szczególności ambroksu - Google Patents

Sposób hydroformylowania 2-podstawionych butadienów oraz wytwarzania ich produktów pochodnych, w szczególności ambroksu

Info

Publication number
PL3319951T3
PL3319951T3 PL16736463T PL16736463T PL3319951T3 PL 3319951 T3 PL3319951 T3 PL 3319951T3 PL 16736463 T PL16736463 T PL 16736463T PL 16736463 T PL16736463 T PL 16736463T PL 3319951 T3 PL3319951 T3 PL 3319951T3
Authority
PL
Poland
Prior art keywords
ambrox
hydroformylation
preparation
same
products derived
Prior art date
Application number
PL16736463T
Other languages
English (en)
Inventor
Julia Strautmann
Stefan Ruedenauer
Christian Rein
Melanie WEINGARTEN
Rocco Paciello
Wolfgang Siegel
Michael Breuer
Peter Hofmann
Sebastian Schmidt
Original Assignee
Basf Se
Ruprecht-Karls-Universität Heidelberg
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 Basf Se, Ruprecht-Karls-Universität Heidelberg filed Critical Basf Se
Publication of PL3319951T3 publication Critical patent/PL3319951T3/pl

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/49Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
    • C07C45/50Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18Catalysts 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
    • B01J31/1845Catalysts 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
    • B01J31/185Phosphites ((RO)3P), their isomeric phosphonates (R(RO)2P=O) and RO-substitution derivatives thereof
    • B01J31/186Mono- or diamide derivatives thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18Catalysts 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
    • B01J31/1845Catalysts 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
    • B01J31/1865Phosphonites (RP(OR)2), their isomeric phosphinates (R2(RO)P=O) and RO-substitution derivatives thereof
    • 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
    • C07C29/14Preparation 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 a —CHO group
    • C07C29/141Preparation 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 a —CHO group with hydrogen or hydrogen-containing gases
    • 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
    • C07C29/56Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by isomerisation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C33/00Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C33/02Acyclic alcohols with carbon-to-carbon double bonds
    • C07C33/025Acyclic alcohols with carbon-to-carbon double bonds with only one double bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00Compounds having —CHO groups
    • C07C47/20Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
    • C07C47/21Unsaturated compounds having —CHO groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/92Naphthofurans; Hydrogenated naphthofurans
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/32Addition reactions to C=C or C-C triple bonds
    • B01J2231/321Hydroformylation, metalformylation, carbonylation or hydroaminomethylation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • C07C2531/18Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Furan Compounds (AREA)
  • Catalysts (AREA)
PL16736463T 2015-07-10 2016-07-08 Sposób hydroformylowania 2-podstawionych butadienów oraz wytwarzania ich produktów pochodnych, w szczególności ambroksu PL3319951T3 (pl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP15176280 2015-07-10
PCT/EP2016/066225 WO2017009205A1 (de) 2015-07-10 2016-07-08 Verfahren zur hydroformylierung von 2-substituierten butadienen und zur herstellung von folgeprodukten davon, speziell von ambrox
EP16736463.7A EP3319951B1 (de) 2015-07-10 2016-07-08 Verfahren zur hydroformylierung von 2-substituierten butadienen und zur herstellung von folgeprodukten davon, speziell von ambrox

Publications (1)

Publication Number Publication Date
PL3319951T3 true PL3319951T3 (pl) 2022-02-28

Family

ID=53773218

Family Applications (1)

Application Number Title Priority Date Filing Date
PL16736463T PL3319951T3 (pl) 2015-07-10 2016-07-08 Sposób hydroformylowania 2-podstawionych butadienów oraz wytwarzania ich produktów pochodnych, w szczególności ambroksu

Country Status (9)

Country Link
US (1) US10315975B2 (pl)
EP (1) EP3319951B1 (pl)
JP (1) JP6852046B2 (pl)
CN (1) CN108026062B (pl)
BR (1) BR112018000481B1 (pl)
ES (1) ES2899823T3 (pl)
MX (1) MX2018000413A (pl)
PL (1) PL3319951T3 (pl)
WO (1) WO2017009205A1 (pl)

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CN109072265A (zh) 2016-02-19 2018-12-21 巴斯夫欧洲公司 高法呢酸的酶促环化
CN109195959B (zh) 2016-05-31 2023-08-18 巴斯夫欧洲公司 四氢吡喃基低碳烷基酯和其使用烯酮化合物的制备
CN109476577A (zh) 2016-07-15 2019-03-15 巴斯夫欧洲公司 由3-甲基-1,5-环十五烷二酮制备14-甲基-16-氧杂双环[10.3.1]十五烯
CN110800150B (zh) 2017-03-31 2022-11-29 株式会社村田制作所 包含电解质稳定材料的非水电解质和电解液、包含它们的二次电池及其用途
MX2019013250A (es) 2017-05-06 2020-01-15 Basf Se 2,3,7-trimetiloct-6-enil acetato y 3,7-dimetil-2-metilen-oct-6-eni l acetato y derivados de estos y su uso como sustancias quimicas aromaticas.
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CN116584093A (zh) 2020-12-09 2023-08-11 三星电子株式会社 Ai编码装置及其操作方法和ai解码装置及其操作方法
ES2989800T3 (es) * 2021-12-17 2024-11-27 Evonik Oxeno Gmbh & Co Kg Procedimiento para la hidroformilación de olefinas con empleo de Pt y yodo

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WO2016097238A1 (en) 2014-12-19 2016-06-23 Basf Se 1-(7,10,10-trimethyl-4-bicyclo(6.2.0)decanyl)ethanone as novel aroma chemical
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CN107109522B (zh) 2015-01-26 2020-02-18 巴斯夫欧洲公司 从混合物中去除放射性核素

Also Published As

Publication number Publication date
BR112018000481B1 (pt) 2022-01-11
EP3319951A1 (de) 2018-05-16
CN108026062A (zh) 2018-05-11
JP6852046B2 (ja) 2021-03-31
BR112018000481A2 (pt) 2018-09-18
WO2017009205A1 (de) 2017-01-19
MX2018000413A (es) 2018-09-06
EP3319951B1 (de) 2021-09-08
CN108026062B (zh) 2022-04-12
US20180273458A1 (en) 2018-09-27
ES2899823T3 (es) 2022-03-14
JP2018528930A (ja) 2018-10-04
US10315975B2 (en) 2019-06-11

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