2-Acetylpyridine benzohydrazide molybdenum complex and preparation method thereof

A kind of technology of acetyl pyridine hydrazide, molybdenum complex, applied in 2-acetyl pyridine benzoyl hydrazide molybdenum complex and preparation field thereof, can solve the problem of unseen molybdenum Schiff base complex and the like problem, to achieve the effect of excellent catalytic performance, low cost and simple operation

Active Publication Date: 2016-02-10
CHINA PETROLEUM & CHEM CORP +1
View PDF5 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But so far, there are no reports of molybdenum Schiff base complexes

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
  • 2-Acetylpyridine benzohydrazide molybdenum complex and preparation method thereof
  • 2-Acetylpyridine benzohydrazide molybdenum complex and preparation method thereof
  • 2-Acetylpyridine benzohydrazide molybdenum complex and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0018] Weigh 10 mmoles of benzoylhydrazine, put it into a round-bottomed flask (50 ml) containing 20 milliliters of absolute ethanol, heat and stir at 50° C., add 10 mmoles of 2-acetylpyridine after the benzoylhydrazine is completely dissolved, After stirring for 1 hour, it was allowed to stand still, and white needle-like crystals precipitated after 7 days. Filtrate with suction and wash with a small amount of ethanol to obtain 2-acetylpyridine benzohydrazine Schiff base complex.

[0019] Weigh 5mmol of 2-acetylpyridinebenzohydrazide Schiff base complex, put it into a round-bottomed flask (50ml) containing 15ml of absolute ethanol, heat and stir at 75°C, and wait until 2-acetylpyridinebenzohydrazide Add 5mmol of molybdenum acetylacetonate after complete dissolution, orange powder is precipitated, continue to heat and stir for 2 hours, filter with suction, wash with ethanol, and dry in vacuum at 40°C to obtain an orange powder product. Its structural formula is as follows, and...

Embodiment 2

[0022] Weigh 10 mmoles of benzoylhydrazine, put it into a round-bottomed flask (50 ml) containing 20 milliliters of pyridine, heat and stir at 50° C., add 10 mmoles of 2-acetylpyridine after the benzoylhydrazide is completely dissolved, and stir for 1 After standing for one hour, white needle-like crystals precipitated after 7 days. Filtrate with suction and wash with a small amount of ethanol to obtain 2-acetylpyridine benzohydrazine Schiff base complex.

[0023] Weigh 5mmol of 2-acetylpyridinebenzohydrazide Schiff base complex, put it into a round-bottomed flask (50ml) containing 15ml of pyridine, heat and stir at 75°C until 2-acetylpyridinebenzohydrazide is completely dissolved Then add 5mmol of molybdenum acetylacetonate, orange powder is precipitated, continue to heat and stir for 2 hours, then suction filter, wash with pyridine and dry in vacuum at 40°C to obtain the product, its structural formula is as follows, its infrared analysis spectrum and figure 1 resemblance. ...

Embodiment 3

[0026] Take tert-butyl hydroperoxide, n-propanol and the 2-acetylpyridine benzohydrazide molybdenum complex synthesized in [Example 1] and put them into a high-pressure reactor, and start heating and stirring after sealing the reactor. When the preset 100°C is reached, the high-pressure pump pumps in propylene, and the amount of propylene is determined by the pumped volume. Reaction timing, after reaching 2 hours, take off the reactor, cool to 10-15°C with ice water, and take the liquid phase into a frozen sampler. Continue to freeze the sampler at minus 20°C for 30 minutes, then unscrew the air valve, slowly release the propylene in the sampler, open the sampler, quickly transfer the remaining liquid to the chromatographic sampling bottle, seal it, and perform chromatographic analysis.

[0027] Reaction conditions: reaction temperature 100°C, reaction time 2 hours, rotating speed 540rpm, tert-butyl hydroperoxide (TBHP) addition 70 millimoles, n-propanol addition 50 millimoles...

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

No PUM Login to view more

Abstract

The invention relates to a 2-acetylpyridine benzoyl hydrazine molybdenum complex and a preparation method thereof, mainly solving the problem that a molybdenum Schiff alkali coordination compound is undisclosed in previous patents. The technical scheme of the invention is adopted to solve the problem, and in the technical scheme, the chemical structural formula of the 2-acetylpyridine benzoyl hydrazine molybdenum complex is shown in the specification, wherein R1 is selected from -OHR2 or R2 is CnH2n+1, and n is 2-10. The preparation method can be applied to the industrial production of the 2-acetylpyridine benzoyl hydrazine molybdenum complex.

Description

technical field [0001] The invention relates to a 2-acetylpyridine benzohydrazide molybdenum complex and a preparation method thereof. Background technique [0002] Schiff base refers to a class of organic compounds containing imine or azimine characteristic groups (-RC=N-), which are formed by condensation of carbonyl and amino groups of aldehydes and ketones under certain conditions. Due to the hyperconjugation between the C=N bond and the benzene ring, such compounds are generally relatively stable. The benzene ring contains Schiff bases with coordination functional groups such as -OH and -N. The intramolecular hydrogen bonding makes it have a rigid structure, and it is very easy to form complexes with high-valent metals as multi-dentate ligands. Therefore, Schiff bases occupy an important position in coordination chemistry. [0003] Schiff bases are an important class of organic synthesis reagents and intermediates. Schiff base compounds and their metal complexes have...

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): C07F11/00B01J31/22C07D301/19C07D303/04
Inventor 王戈宋纪元陶乔杨穆谭丽高焕新金国杰
Owner CHINA PETROLEUM & CHEM CORP
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap