Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Synthesis method of (E)-beta-nitrostyrene

A technology of nitrostyrene and a synthesis method, which is applied in the field of synthesis of -β-nitrostyrene, can solve the problems of difficult industrial application, low reaction efficiency, low yield and the like, and achieves the advantages of being beneficial to industrial production, simplifying Process steps, effect of high stereoselectivity

Active Publication Date: 2017-08-29
大庆三聚能源净化有限公司
View PDF7 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Such as Chinese patent (CN106083597A) discloses a kind of synthetic method of conjugated nitroalkene, under the condition that diamine exists, utilize fatty aldehyde and the nitro group of nitroalkane to carry out aldol condensation reaction, by adding acid in the reaction process The elimination reaction of the conjugated nitroalkene carried out (as reaction 2); This method uses diamine as the catalyzer of nitro aldol condensation reaction, reduces side reaction generation, improves product yield, but this reaction step is many, has a large amount of acidity Waste liquid generation, polluting the environment
Chinese patent (CN 104710315 A) discloses a green synthesis method of α,β-unsaturated nitroolefin compounds (such as reaction 3), which uses functionalized ionic liquid and water as the catalytic system, aromatic aldehyde and nitroalkane Microwave heating reaction can make the reaction conditions mild and increase the reaction yield; however, the cost of ionic liquid used in this method is high and it is difficult to be applied industrially
The patent (CN1438977A) of Sabao Group Company of Italy's application in China discloses that styrene derivatives are used as raw materials, and the mixture of inorganic nitrite and iodine in the presence of peroxides is a nitrating reagent to synthesize nitrostyrene compounds; the method Due to the use of oxidants, the amount of iodine used in the process of nitrating olefins is greatly reduced, thereby improving the yield of the product to a certain extent and simplifying the process steps. However, these methods all use nitrite as the nitrating reagent, which is harmful to the environment and human body.
At present, there are still some nitrogen-containing oxides used as nitrating reagents to directly carry out nitration reaction with alkene compounds under the catalysis of metal nickel oxides to obtain nitroalkene derivatives (such as reaction 4). This method adopts gas-liquid reaction mode, the reaction efficiency is low, and toxic gas will be produced, and the yield yield is not high

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
  • Synthesis method of (E)-beta-nitrostyrene
  • Synthesis method of (E)-beta-nitrostyrene
  • Synthesis method of (E)-beta-nitrostyrene

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] Styrene (0.5mmol), NH 4 I (1.5 equivalents, 0.75mmol, 108mg), TBHP (70% H 2 O, 6.0 equiv, 3.0 mmol, 384 mg), TPPFeCl (3-5% on molar styrene) and acetonitrile (2 mL) were added to a sealed tube. Acetonitrile was added first, followed by styrene, NH 4 I and TPPFeCl, and finally TBHP. The reaction was stirred vigorously at 120 °C for 6 hours and monitored by TLC. After the reaction was complete, the mixture was cooled to room temperature, then filtered and washed with ethyl acetate (EA). Finally, the filtrate was concentrated with a rotary evaporator, and purified by column chromatography with silica gel (200-300 mesh) using petroleum ether (PE) / ethyl acetate (EA) as eluent.

[0039] Yellow solid: 82% (61mg). 1 H NMR (400MHz, CDCl 3 )δ8.01(d, J=13.7Hz, 1H), 7.63–7.53(m, 3H), 7.47(tdd, J=8.5, 5.2, 3.6Hz, 3H). 13 C NMR (101MHz, CDCl 3 )δ139.04,137.06,132.11,130.01,129.35,129.10.GC-MS(m / z):149.+.

[0040] Compared with experimental group 1:

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 discloses a synthesis method of (E)-beta-nitrostyrene. In the method, the (E)-beta-nitrostyrene is produced through a one-pot reaction to styrene in a system comprising tetraaryl ferric porphyrin (III), ammonium halide salt and tert-butyl hydroperoxide. The method can synthesize the (E)-beta-nitrostyrene, which has high E-stereoscopic selectivity, under gentle reaction conditions at high yield.

Description

technical field [0001] The present invention relates to a kind of synthetic method of (E)-beta-nitrostyrene, particularly a kind of styrene in the system containing tetraaryl porphyrin iron (III), ammonium halide salt and tert-butyl hydroperoxide The invention discloses a method for synthesizing (E)-beta-nitrostyrene with high yield and high selectivity in one pot reaction, belonging to the field of organic synthesis. Background technique [0002] α,β-Unsaturated nitroalkenes are a class of biologically active compounds. For example, unsaturated nitro fatty acids are a new class of endogenous anti-inflammatory mediators; unsaturated nitrooleic acid can prevent renal ischemia and reperfusion injury in rats. At the same time, α,β-unsaturated nitroalkenes are an important class of drugs and organic intermediate compounds, which can be easily converted into a variety of different compounds and play an important role in many fields. For example, β-nitrostyrene is an intermediat...

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 Applications(China)
IPC IPC(8): C07C201/08C07C205/04
CPCC07C201/08C07C205/04
Inventor 郭灿城曹重仲郭欣
Owner 大庆三聚能源净化有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products