Unlock instant, AI-driven research and patent intelligence for your innovation.

Method for preparing decanal

A technology of decanal and decenal, which is applied to the preparation of carbon-based compounds, chemical instruments and methods, and the preparation of organic compounds, and can solve the problems of high price and high energy consumption

Active Publication Date: 2022-07-12
CHINA PETROLEUM & CHEM CORP +1
View PDF9 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although the method described in this document has a high selectivity to the conversion rate of decenal and decanal, the active component of the catalyst required for the reaction is mainly Pt, and it is imported from abroad, which is expensive, and the temperature required for the reaction Above 100°C, high energy consumption

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for preparing decanal
  • Method for preparing decanal
  • Method for preparing decanal

Examples

Experimental program
Comparison scheme
Effect test

preparation example 1

[0043] This preparation example provides a composite catalyst.

[0044] (1) Weigh 3g (0.03mol) of polyvinyl imidazole (PVIM) and dissolve it in 200ml of methanol, and add 50ml of peroxymolybdic acid (self-made, commercially available molybdenum powder is dissolved in 30% hydrogen peroxide) dropwise under stirring conditions. A solution of methanol at a concentration of 0.1 mmol / ml, a solid material immediately appeared in the solution. After the dropwise addition was completed, stirring was maintained for 4 h. Finally, after vacuum filtration and methanol washing for 3 times, it was dried at 80 °C for 8 h to obtain peroxymolybdic acid-polyvinylimidazole polymer, denoted as PMo-1.

[0045] (2) 2 g of PMo-1 obtained in Preparation Example 1 was weighed and dispersed in 20 ml of methanol, and 40 ml of palladium nitrate methanol solution with a palladium concentration of 0.5 mg / ml was added dropwise under stirring. After the dropwise addition was completed, stirring was maintain...

preparation example 2

[0049] This preparation example provides a composite catalyst.

[0050] (1) 2 g of PMo-1 obtained in Preparation Example 1 was weighed and dispersed in 20 ml of methanol, and 40 ml of palladium nitrate methanol solution with a palladium concentration of 0.05 mg / ml was added dropwise under stirring. After the dropwise addition was completed, stirring was maintained for 4 h. Finally, after vacuum filtration and methanol washing for 3 times, drying at 80°C for 8 h was obtained to obtain a palladium-peroxymolybdic acid-polyvinylimidazole composite catalyst with a Pd loading of 0.1%, number A1-2.

[0051] (2) The schematic structural formula of A1-2 is shown in formula I.

preparation example 3

[0053] This preparation example provides a composite catalyst.

[0054] (1) Weigh 3.76g (0.04mol) of polyvinylimidazole (PVIM) and dissolve it in 200ml of methanol, add 100ml of peroxymolybdic acid (self-made, commercially available molybdenum powder is dissolved in 30% hydrogen peroxide) dropwise with stirring ) at a concentration of 0.1 mmol / ml in methanol, a solid material immediately appeared in the solution. After the dropwise addition was completed, stirring was maintained for 4 h. Finally, after vacuum filtration and methanol washing for 3 times, it was dried at 80 °C for 8 h to obtain a peroxymolybdic acid-polyvinylimidazole polymer, which was denoted as PMo-2.

[0055] (2) 2 g of PMo-2 obtained in Preparation Example 3 was weighed and dispersed in 20 ml of methanol, and 40 ml of palladium nitrate methanol solution containing palladium concentration of 0.5 mg / ml was added dropwise under stirring. After the dropwise addition was completed, stirring was maintained for ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
particle sizeaaaaaaaaaa
concentrationaaaaaaaaaa
Login to View More

Abstract

The invention belongs to the technical field of catalytic hydrogenation, and relates to a method for preparing decanal. The method includes the following steps: in the presence of hydrogen, a composite catalyst, decaenal and an organic solvent are contacted and reacted to obtain a product containing decanal; the composite catalyst comprises a polymer matrix cross-linked by a polybasic acid and a metal active component The macromolecular matrix is ​​a macromolecular polymer containing a nitrogen-containing heterocyclic side group, and the nitrogen atom in the nitrogen-containing heterocyclic side group has a lone pair of electrons, which can firmly support metal active components through coordination bonds. The method for preparing decanal provided by the invention can improve the selectivity of decanal hydrogenation to form decanal, suppress the generation of decanol, and the catalyst used in the method is low in cost and low in reaction temperature.

Description

technical field [0001] The invention belongs to the technical field of catalytic hydrogenation, and more particularly, relates to a method for preparing decanal. Background technique [0002] Decanal is an important organic raw material and spice, which naturally exists in citrus, lemon, grapefruit, tomato, strawberry and other fruits. Due to the high cost and low yield of extracting decanal from natural plants, decanal is mostly produced by industrial synthesis. [0003] The existing route of producing decanal mainly includes: (1) trimerization of propylene or oligomeric cutting of propylene and butene, to obtain the olefin of C9, then through oxo, hydrogenation, to generate decanal; (2) butylene The hydroformylation of alkenes produces valeraldehyde, which is then condensed to form decanal, and then hydrogenated to form decanal. [0004] At present, most researches focus on the hydrogenation of decenaldehyde to produce decanol. For example, the patent document CN1011858...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C07C47/02C07C45/62B01J31/22
CPCC07C45/62B01J31/1815B01J2531/824B01J35/394C07C47/02Y02P20/584
Inventor 陈勇鲁树亮徐洋吴佳佳郝雪松
Owner CHINA PETROLEUM & CHEM CORP