[go: up one dir, main page]

MX2024001309A - Metodo para producir aldehidos grasos y derivados de los mismos. - Google Patents

Metodo para producir aldehidos grasos y derivados de los mismos.

Info

Publication number
MX2024001309A
MX2024001309A MX2024001309A MX2024001309A MX2024001309A MX 2024001309 A MX2024001309 A MX 2024001309A MX 2024001309 A MX2024001309 A MX 2024001309A MX 2024001309 A MX2024001309 A MX 2024001309A MX 2024001309 A MX2024001309 A MX 2024001309A
Authority
MX
Mexico
Prior art keywords
derivatives
fatty aldehydes
producing fatty
aldehydes
purification
Prior art date
Application number
MX2024001309A
Other languages
English (en)
Inventor
Anders Gabrielsson
Andrea Mazziotta
Original Assignee
Fmc Agricultural Solutions 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 Fmc Agricultural Solutions As filed Critical Fmc Agricultural Solutions As
Publication of MX2024001309A publication Critical patent/MX2024001309A/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/37—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of >C—O—functional groups to >C=O 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
    • 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
    • B01J31/1805—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 nitrogen
    • B01J31/181—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
    • 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
    • B01J31/1805—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 nitrogen
    • B01J31/181—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
    • B01J31/1815—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine with more than one complexing nitrogen atom, e.g. bipyridyl, 2-aminopyridine
    • 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
    • B01J31/22—Organic complexes
    • B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208—Oxygen, e.g. acetylacetonates
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/29—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/78—Separation; Purification; Stabilisation; Use of additives
    • C07C45/80—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00—Compounds having —CHO groups
    • C07C47/02—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen
    • 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
    • B01J2231/70—Oxidation reactions, e.g. epoxidation, (di)hydroxylation, dehydrogenation and analogues
    • B01J2231/76—Dehydrogenation
    • B01J2231/763—Dehydrogenation of -CH-XH (X= O, NH/N, S) to -C=X or -CX triple bond species
    • 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
    • B01J2531/001—General concepts, e.g. reviews, relating to catalyst systems and methods of making them, the concept being defined by a common material or method/theory
    • B01J2531/002—Materials
    • B01J2531/004—Ligands
    • 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
    • B01J2531/10—Complexes comprising metals of Group I (IA or IB) as the central metal
    • B01J2531/16—Copper

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)
  • Fats And Perfumes (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

La presente invención se refiere a un método para convertir alcoholes a aldehídos, en particular alcoholes grasos a aldehídos grasos, tal método utiliza un catalizador, en donde el método es capaz de proporcionar alta conversión de tal alcohol, por ejemplo en una gran escala, en donde la reacción y la purificación utilizan una cantidad relativamente pequeña de solvente, y en donde la purificación es capaz de eliminar el catalizador del producto aldehído.
MX2024001309A 2021-08-06 2022-08-02 Metodo para producir aldehidos grasos y derivados de los mismos. MX2024001309A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP21190097 2021-08-06
EP22161123 2022-03-09
PCT/EP2022/071672 WO2023012151A1 (en) 2021-08-06 2022-08-02 Method for producing fatty aldehydes and derivatives thereof

Publications (1)

Publication Number Publication Date
MX2024001309A true MX2024001309A (es) 2024-05-17

Family

ID=83113041

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2024001309A MX2024001309A (es) 2021-08-06 2022-08-02 Metodo para producir aldehidos grasos y derivados de los mismos.

Country Status (12)

Country Link
US (1) US20240327324A1 (es)
EP (1) EP4380916A1 (es)
JP (1) JP2024537933A (es)
KR (1) KR20240042428A (es)
AR (1) AR126717A1 (es)
AU (1) AU2022321753A1 (es)
CA (1) CA3225388A1 (es)
CL (1) CL2024000256A1 (es)
IL (1) IL309880A (es)
MX (1) MX2024001309A (es)
TW (1) TW202313546A (es)
WO (1) WO2023012151A1 (es)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2025027140A1 (en) 2023-08-02 2025-02-06 FMC Agricultural Solutions A/S N-alkoxyamine marker and processes

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5155280A (en) 1991-09-30 1992-10-13 Shell Oil Company Process for the oxidation of alcohols to aldehydes
EP3313997B1 (en) 2015-06-26 2020-02-05 Danmarks Tekniske Universitet Method for production of moth pheromones in yeast
ES2930358T3 (es) 2016-12-16 2022-12-09 Univ Danmarks Tekniske Producción de alcoholes grasos desaturados y acetatos de acilo grasos desaturados en levaduras
EP3555268B1 (en) 2016-12-16 2021-05-26 Danmarks Tekniske Universitet Methods for producing fatty alcohols and derivatives thereof in yeast
US20230332096A1 (en) 2019-02-19 2023-10-19 Biophero Aps Methods and cell factories for producing insect pheromones
AU2020370542A1 (en) 2019-10-22 2022-04-28 FMC Agricultural Solutions A/S Improved methods for production, recovery and secretion of hydrophobic compounds in a fermentation
BR112022012109A2 (pt) 2019-12-20 2022-12-13 Biophero Aps Célula de levedura capaz de produzir e8,e10-dodecadienil coenzima a e opcionalmente e8,e10-dodecadien-1-ol, e, método para produzir e8,e10-dodecadienil coenzima a e opcionalmente e8,e10-dodecadien-1-ol em uma célula de levedura

Also Published As

Publication number Publication date
JP2024537933A (ja) 2024-10-17
IL309880A (en) 2024-03-01
WO2023012151A1 (en) 2023-02-09
US20240327324A1 (en) 2024-10-03
AU2022321753A1 (en) 2024-01-25
KR20240042428A (ko) 2024-04-02
TW202313546A (zh) 2023-04-01
CA3225388A1 (en) 2023-02-09
EP4380916A1 (en) 2024-06-12
CL2024000256A1 (es) 2024-06-07
AR126717A1 (es) 2023-11-08

Similar Documents

Publication Publication Date Title
JP2004536880A5 (es)
RU2439047C2 (ru) Способ получения 1,2-пропандиола гидрогенолизом глицерина
MX2024001309A (es) Metodo para producir aldehidos grasos y derivados de los mismos.
Shi et al. Straightforward selective synthesis of linear 1-O-alkyl glycerol and di-glycerol monoethers
JP6927533B2 (ja) アルコールの直鎖及び分枝官能化アルカンへの変換
FR2939791A1 (fr) Procede de preparation d'acroleine a partir de glycerol ou de glycerine brute
RU2436761C2 (ru) Способ получения 1,2-пропандиола гидрогенолизом глицерина
Hermans et al. Solvent‐and metal‐free ketonization of fatty acid methyl esters and triacylglycerols with nitrous oxide
CN102030612B (zh) 利用含醇废液制备正丁醇的方法
MY152802A (en) Method for the production of fatty alcohols
RU2008126388A (ru) Способ получнеия пропилена
KR20160063124A (ko) 불포화 알콜 제조방법
JP6084336B2 (ja) アリルアルコールの製造方法及びこれにより製造されたアリルアルコール
JP2011506419A (ja) １，２−プロパンジオールの製造方法
EP2236487A3 (en) Processes for producing levosandal and levosandol
Corberán et al. Heterogeneous selective oxidation of fatty alcohols: Oxidation of 1-tetradecanol as a model substrate
EP2616452A1 (fr) Procede de fabrication de dioxolane
MY209257A (en) Process for hydrogenation of c13 aldehydes in at least two hydrogenation stages
FR2980791A1 (fr) Procede de preparation d'un melange d'alcools
JP5177759B2 (ja) 多価アルコールからの環状エーテル及びヒドロキシケトンの製造方法
MX2022013202A (es) Proceso para producir esteres de (met)acrilato de hidroxialquilo mediante escision oxidativa de acetales de metacroleina.
RU2102377C1 (ru) Способ получения 4-циклогексил-4-метилпентанона-2
CN109608426B (zh) 一种以生产柠檬醛的废液为原料合成铃兰吡喃的方法
AU2012370043B2 (en) Process for synthesis of alcohols
CN101139250A (zh) 一种合成正丁醇的方法