AR126717A1 - Método para producir aldehídos grasos y derivados de los mismos - Google Patents
Método para producir aldehídos grasos y derivados de los mismosInfo
- Publication number
- AR126717A1 AR126717A1 ARP220102108A ARP220102108A AR126717A1 AR 126717 A1 AR126717 A1 AR 126717A1 AR P220102108 A ARP220102108 A AR P220102108A AR P220102108 A ARP220102108 A AR P220102108A AR 126717 A1 AR126717 A1 AR 126717A1
- Authority
- AR
- Argentina
- Prior art keywords
- fatty
- weight
- alcohol
- reaction mixture
- aldehyde
- Prior art date
Links
- 150000002192 fatty aldehydes Chemical class 0.000 title abstract 5
- 229940053991 aldehydes and derivative Drugs 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000002191 fatty alcohols Chemical class 0.000 abstract 5
- 238000000034 method Methods 0.000 abstract 5
- 239000011541 reaction mixture Substances 0.000 abstract 4
- 239000003054 catalyst Substances 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 150000001299 aldehydes Chemical class 0.000 abstract 2
- 229910052802 copper Inorganic materials 0.000 abstract 2
- 239000010949 copper Substances 0.000 abstract 2
- 238000000746 purification Methods 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 1
- 229930195729 fatty acid Natural products 0.000 abstract 1
- 239000000194 fatty acid Substances 0.000 abstract 1
- 150000004665 fatty acids Chemical class 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000012429 reaction media Substances 0.000 abstract 1
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
- C07C45/29—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
- C07C45/27—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
- C07C45/78—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
Un método para convertir alcoholes en aldehídos, en particular alcoholes grasos, en aldehídos grasos, donde dicho método utiliza un catalizador, y el método es capaz de proveer una alta conversión de dicho alcohol, por ejemplo a gran escala, donde en la reacción y la purificación se utiliza una cantidad relativamente pequeña de solvente, y donde la purificación es capaz de eliminar el catalizador del producto aldehído. Reivindicación 1: Un método para la conversión a gran escala de un alcohol graso en un aldehído graso, caracterizado porque dicho método comprende los siguientes pasos: a) proveer una mezcla de reacción que comprende por lo menos 1 kilogramo de alcohol graso, un catalizador que comprende una fuente de cobre, por lo menos 1 kilogramo de solvente y un material que absorbe o adsorbe agua, y b) disolver por lo menos 0,01 mmol de O₂ por minuto por μmol de cobre en la mezcla de reacción o por lo menos 0,001 mmol de O₂ por minuto por μmol (cantidad inicial) de alcohol graso en la mezcla de reacción a la mezcla de reacción alimentando un gas o un líquido que comprende O₂ al medio de reacción para oxidar de esa manera más del 50% en peso del alcohol graso a aldehído graso y menos del 50% en peso a ácido graso. Reivindicación 25: Una composición caracterizada porque comprende más del 93% en peso de aldehído graso, menos del 7% en peso de alcohol graso y menos del 2% en peso de agua.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP21190097 | 2021-08-06 | ||
| EP22161123 | 2022-03-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR126717A1 true AR126717A1 (es) | 2023-11-08 |
Family
ID=83113041
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP220102108A AR126717A1 (es) | 2021-08-06 | 2022-08-05 | Método para producir aldehídos 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)
| 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)
| 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 |
| ES2789823T3 (es) | 2015-06-26 | 2020-10-26 | Univ Danmarks Tekniske | Procedimiento de producción de feromonas de polilla en levadura |
| EP3555268B1 (en) | 2016-12-16 | 2021-05-26 | Danmarks Tekniske Universitet | Methods for producing fatty alcohols and derivatives thereof in yeast |
| WO2018109167A1 (en) | 2016-12-16 | 2018-06-21 | Danmarks Tekniske Universitet | Production of desaturated fatty alcohols and desaturated fatty acyl acetates in yeast |
| US20230332096A1 (en) | 2019-02-19 | 2023-10-19 | Biophero Aps | Methods and cell factories for producing insect pheromones |
| BR112022006218A2 (pt) | 2019-10-22 | 2022-06-28 | Biophero Aps | Método para produzir um composto hidrofóbico, para aumentar o título de um composto hidrofóbico, para aumentar a secreção de um composto hidrofóbico e para monitorar a presença de praga ou romper a reprodução de praga, e, composto hidrofóbico |
| CN115103900A (zh) | 2019-12-20 | 2022-09-23 | 费罗生物公司 | 产生e8,e10-十二碳二烯基辅酶a、可得蒙及其衍生物的酵母细胞和方法 |
-
2022
- 2022-08-02 WO PCT/EP2022/071672 patent/WO2023012151A1/en not_active Ceased
- 2022-08-02 US US18/293,550 patent/US20240327324A1/en active Pending
- 2022-08-02 AU AU2022321753A patent/AU2022321753A1/en active Pending
- 2022-08-02 MX MX2024001309A patent/MX2024001309A/es unknown
- 2022-08-02 KR KR1020247003847A patent/KR20240042428A/ko active Pending
- 2022-08-02 EP EP22760913.8A patent/EP4380916A1/en active Pending
- 2022-08-02 IL IL309880A patent/IL309880A/en unknown
- 2022-08-02 CA CA3225388A patent/CA3225388A1/en active Pending
- 2022-08-02 JP JP2024503484A patent/JP2024537933A/ja active Pending
- 2022-08-05 TW TW111129581A patent/TW202313546A/zh unknown
- 2022-08-05 AR ARP220102108A patent/AR126717A1/es unknown
-
2024
- 2024-01-29 CL CL2024000256A patent/CL2024000256A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP4380916A1 (en) | 2024-06-12 |
| CA3225388A1 (en) | 2023-02-09 |
| MX2024001309A (es) | 2024-05-17 |
| US20240327324A1 (en) | 2024-10-03 |
| KR20240042428A (ko) | 2024-04-02 |
| WO2023012151A1 (en) | 2023-02-09 |
| TW202313546A (zh) | 2023-04-01 |
| AU2022321753A1 (en) | 2024-01-25 |
| IL309880A (en) | 2024-03-01 |
| JP2024537933A (ja) | 2024-10-17 |
| CL2024000256A1 (es) | 2024-06-07 |
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