MX2018011232A - Procedimiento para producir prenol y prenal a partir de isoprenol. - Google Patents
Procedimiento para producir prenol y prenal a partir de isoprenol.Info
- Publication number
- MX2018011232A MX2018011232A MX2018011232A MX2018011232A MX2018011232A MX 2018011232 A MX2018011232 A MX 2018011232A MX 2018011232 A MX2018011232 A MX 2018011232A MX 2018011232 A MX2018011232 A MX 2018011232A MX 2018011232 A MX2018011232 A MX 2018011232A
- Authority
- MX
- Mexico
- Prior art keywords
- methyl
- prenal
- isoprenol
- butenol
- procedure
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/56—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by isomerisation
-
- 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
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
- B01J21/04—Alumina
-
- 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
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
- B01J21/08—Silica
-
- 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
- B01J23/44—Palladium
-
- 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/48—Silver or gold
- B01J23/52—Gold
-
- 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
- C07C45/38—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 being a primary hydroxyl group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C33/00—Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C33/02—Acyclic alcohols with carbon-to-carbon double bonds
- C07C33/025—Acyclic alcohols with carbon-to-carbon double bonds with only one double bond
- C07C33/03—Acyclic alcohols with carbon-to-carbon double bonds with only one double bond in beta-position, e.g. allyl alcohol, methallyl alcohol
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
- C07C47/21—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic 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)
- Catalysts (AREA)
Abstract
La presente invención se refiere a un procedimiento para preparar 3-metil-2-butenol (prenol) y 3-metil-2-butenal (prenal) a partir de 3-metil-3-butenol (isoprenol), en el que el 3-metil-3-butenol es sometido a una isomerización catalítica por medio de un catalizador de Pd con soporte de carbono en presencia de una mezcla de gases que contiene 1% a 15% en volumen de oxígeno, con lo cual se obtiene una primera mezcla de productos, y esa primera mezcla de productos es sometida a una deshidrogenación oxidativa por medio de un catalizador de Pd que contiene SiO2 y/o Al2O3 como material de soporte, o por medio de un catalizador de Pd/Au con soporte de carbono en presencia de una mezcla de gases que contiene de 5% a 25% en volumen de oxígeno.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP16160410 | 2016-03-15 | ||
| PCT/EP2017/055922 WO2017157897A1 (de) | 2016-03-15 | 2017-03-14 | Verfahren zur herstellung von prenol und prenal aus isoprenol |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MX2018011232A true MX2018011232A (es) | 2018-11-22 |
| MX388816B MX388816B (es) | 2025-03-20 |
Family
ID=55532204
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2018011232A MX388816B (es) | 2016-03-15 | 2017-03-14 | Procedimiento para producir prenol y prenal a partir de isoprenol. |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10414707B2 (es) |
| EP (1) | EP3429982B1 (es) |
| JP (1) | JP6816162B6 (es) |
| CN (1) | CN108779054B (es) |
| MX (1) | MX388816B (es) |
| MY (1) | MY188612A (es) |
| WO (1) | WO2017157897A1 (es) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110368938B (zh) * | 2019-08-09 | 2022-02-11 | 中触媒新材料股份有限公司 | 一种用于3-甲基-2-丁烯-1-醇合成异戊烯醛催化剂的制备方法 |
| CN110407680B (zh) * | 2019-08-20 | 2022-08-02 | 万华化学集团股份有限公司 | 一种制备异戊烯醛的方法 |
| US10974225B1 (en) * | 2020-01-17 | 2021-04-13 | Zhejiang Nhu Company Ltd. | Metal oxide coated ceramic corrugated plate catalyst, preparation and application in preparation of key intermediates of citral |
| CN111992220B (zh) * | 2020-05-31 | 2023-05-26 | 南京克米斯璀新能源科技有限公司 | 一种异戊烯醛的制备方法 |
| CN112125783B (zh) * | 2020-09-10 | 2022-04-22 | 万华化学集团股份有限公司 | 一种光催化制备3-甲基-2-丁烯醇的方法 |
| CN114380677B (zh) * | 2020-10-16 | 2023-12-19 | 万华化学集团股份有限公司 | 一种3-甲基-2-丁烯醛的制备方法 |
| CN114349613B (zh) * | 2022-01-11 | 2023-05-26 | 万华化学集团股份有限公司 | 一种3-甲基-2-丁烯醛的制备方法 |
| WO2025108976A2 (en) * | 2023-11-20 | 2025-05-30 | Basf Se | Process for isomerizing an ethylenically unsaturated alcohol |
| WO2025114332A1 (en) | 2023-11-27 | 2025-06-05 | Basf Se | Process for isomerizing an ethylenically unsaturated alcohol in a cascade of reactors |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008037693A1 (de) * | 2006-09-26 | 2008-04-03 | Basf Se | Kontinuierliches verfahren zur herstellung von citral |
| DE102008011767B4 (de) | 2008-02-28 | 2012-07-26 | Basf Se | Verfahren zur Herstellung von olefinisch ungesättigten Carbonylverbindungen durch oxidative Dehydrierung von Alkoholen |
-
2017
- 2017-03-14 EP EP17709715.1A patent/EP3429982B1/de active Active
- 2017-03-14 WO PCT/EP2017/055922 patent/WO2017157897A1/de not_active Ceased
- 2017-03-14 MY MYPI2018001530A patent/MY188612A/en unknown
- 2017-03-14 US US16/084,285 patent/US10414707B2/en active Active
- 2017-03-14 MX MX2018011232A patent/MX388816B/es unknown
- 2017-03-14 CN CN201780017069.7A patent/CN108779054B/zh active Active
- 2017-03-14 JP JP2018548222A patent/JP6816162B6/ja active Active
Also Published As
| Publication number | Publication date |
|---|---|
| CN108779054B (zh) | 2022-01-07 |
| EP3429982B1 (de) | 2020-06-10 |
| MY188612A (en) | 2021-12-22 |
| JP6816162B2 (ja) | 2021-01-20 |
| WO2017157897A1 (de) | 2017-09-21 |
| US20190077736A1 (en) | 2019-03-14 |
| EP3429982A1 (de) | 2019-01-23 |
| MX388816B (es) | 2025-03-20 |
| JP6816162B6 (ja) | 2021-02-10 |
| CN108779054A (zh) | 2018-11-09 |
| JP2019510018A (ja) | 2019-04-11 |
| US10414707B2 (en) | 2019-09-17 |
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