SG11201406503VA - Process for the chemoselective reduction of terminally saturated carboxylic esters - Google Patents

Process for the chemoselective reduction of terminally saturated carboxylic esters

Info

Publication number
SG11201406503VA
SG11201406503VA SG11201406503VA SG11201406503VA SG11201406503VA SG 11201406503V A SG11201406503V A SG 11201406503VA SG 11201406503V A SG11201406503V A SG 11201406503VA SG 11201406503V A SG11201406503V A SG 11201406503VA SG 11201406503V A SG11201406503V A SG 11201406503VA
Authority
SG
Singapore
Prior art keywords
carboxylic esters
saturated carboxylic
chemoselective reduction
terminally saturated
terminally
Prior art date
Application number
SG11201406503VA
Other languages
English (en)
Inventor
Roger Wilhelm Geisser
Andreas Goeke
Fridtjof Schroeder
Original Assignee
Givaudan Sa
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 Givaudan Sa filed Critical Givaudan Sa
Publication of SG11201406503VA publication Critical patent/SG11201406503VA/en

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
    • 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
    • B01J31/189Catalysts 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 containing both nitrogen and phosphorus as complexing atoms, including e.g. phosphino moieties, in one at least bidentate or bridging ligand
    • 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
    • B01J2231/60Reduction reactions, e.g. hydrogenation
    • B01J2231/64Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
    • B01J2231/641Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0238Complexes comprising multidentate ligands, i.e. more than 2 ionic or coordinative bonds from the central metal to the ligand, the latter having at least two donor atoms, e.g. N, O, S, P
    • B01J2531/0241Rigid ligands, e.g. extended sp2-carbon frameworks or geminal di- or trisubstitution
    • B01J2531/0255Ligands comprising the N2S2 or N2P2 donor atom set, e.g. diiminodithiolates or diiminodiphosphines with complete pi-conjugation between all donor centres
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/821Ruthenium

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
SG11201406503VA 2012-05-16 2013-05-16 Process for the chemoselective reduction of terminally saturated carboxylic esters SG11201406503VA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB1208589.0A GB201208589D0 (en) 2012-05-16 2012-05-16 Improvements in or relating to organic compounds
PCT/EP2013/060150 WO2013171302A1 (en) 2012-05-16 2013-05-16 Process for the chemoselective reduction of terminally saturated carboxylic esters

Publications (1)

Publication Number Publication Date
SG11201406503VA true SG11201406503VA (en) 2014-11-27

Family

ID=46458913

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201406503VA SG11201406503VA (en) 2012-05-16 2013-05-16 Process for the chemoselective reduction of terminally saturated carboxylic esters

Country Status (10)

Country Link
US (1) US9193651B2 (enExample)
EP (1) EP2850050B1 (enExample)
JP (1) JP6279552B2 (enExample)
CN (1) CN104284875B (enExample)
BR (1) BR112014028156A2 (enExample)
GB (1) GB201208589D0 (enExample)
IN (1) IN2014DN08413A (enExample)
MX (1) MX363196B (enExample)
SG (1) SG11201406503VA (enExample)
WO (1) WO2013171302A1 (enExample)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR3013047B1 (fr) 2013-11-08 2016-01-01 Pivert Procede de synthese d'esters
JP6483134B2 (ja) 2013-12-18 2019-03-13 フイルメニツヒ ソシエテ アノニムFirmenich Sa Fe/三座配位子錯体によるエステルの水素化
US9416091B1 (en) * 2015-02-04 2016-08-16 Sirrus, Inc. Catalytic transesterification of ester compounds with groups reactive under transesterification conditions
CN105582961B (zh) * 2014-10-24 2018-04-06 中国石油化工股份有限公司 1,4‑环己烷二甲酸二甲酯氢化催化剂
US10501400B2 (en) 2015-02-04 2019-12-10 Sirrus, Inc. Heterogeneous catalytic transesterification of ester compounds with groups reactive under transesterification conditions
AU2016357756B2 (en) 2015-11-18 2021-09-30 Provivi, Inc. Production of fatty olefin derivatives via olefin metathesis
US10428177B2 (en) 2016-06-03 2019-10-01 Sirrus, Inc. Water absorbing or water soluble polymers, intermediate compounds, and methods thereof
JP7153937B2 (ja) 2017-02-17 2022-10-17 プロビビ インコーポレイテッド オレフィンメタセシスによるフェロモンおよび関連材料の合成方法
GB201800276D0 (en) 2018-01-08 2018-02-21 Univ Court Univ St Andrews Maganese-catalysed hydrogenation of esters
EP3994117B1 (de) 2019-07-03 2024-07-03 Basf Se Hydrierung von estern zu alkoholen in gegenwart eines ru-pnn-komplexes

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101137601B (zh) * 2005-04-05 2011-08-10 弗门尼舍有限公司 通过钌/二齿配体的络合物进行的酯的氢化
WO2006106484A1 (en) 2005-04-05 2006-10-12 Firmenich Sa Hydrogenation of esters with ru/tetradentate ligands complexes
CN101541716B (zh) * 2006-11-27 2012-10-03 弗门尼舍有限公司 通过钌/二齿配位体的络合物进行的酯的氢化
JP5849710B2 (ja) * 2011-02-03 2016-02-03 セントラル硝子株式会社 β−フルオロアルコール類の製造方法
EP2744815B1 (en) 2011-08-18 2019-01-16 Goussev, Dmitri Hydrogenation and dehydrogenation catalyst, and methods of making and using the same

Also Published As

Publication number Publication date
MX2014012447A (es) 2015-01-15
BR112014028156A2 (pt) 2017-06-27
US20150152029A1 (en) 2015-06-04
WO2013171302A1 (en) 2013-11-21
US9193651B2 (en) 2015-11-24
IN2014DN08413A (enExample) 2015-05-08
CN104284875B (zh) 2017-10-03
EP2850050B1 (en) 2018-12-12
JP6279552B2 (ja) 2018-02-14
EP2850050A1 (en) 2015-03-25
JP2015520156A (ja) 2015-07-16
MX363196B (es) 2019-03-14
GB201208589D0 (en) 2012-06-27
CN104284875A (zh) 2015-01-14

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