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

Catalyst and preparation method for synthesizing salicylic acid by carboxylation reaction of phenol

A technology of phenol carboxyl group and catalyst, which is applied in the field of catalyst and preparation of phenol carboxylation reaction to synthesize salicylic acid, can solve the problems of harsh reaction conditions, high reaction efficiency, low reaction activity, etc., and achieve simple recycling, high catalytic activity, Strong solubility effect

Active Publication Date: 2022-03-11
SOUTHEAST UNIV
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The catalyst adopted in the present invention overcomes the problems of previous inorganic salt catalysts such as potassium carbonate with low reactivity and harsh reaction conditions. At the same time, compared with other ionic liquid catalysts, the MOFs immobilized ionic liquid catalyst has high reaction efficiency and magnetic nano-core The existence of the catalyst is more convenient for recovery and reuse, so the stability of the catalyst is better

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
  • Catalyst and preparation method for synthesizing salicylic acid by carboxylation reaction of phenol
  • Catalyst and preparation method for synthesizing salicylic acid by carboxylation reaction of phenol
  • Catalyst and preparation method for synthesizing salicylic acid by carboxylation reaction of phenol

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] Preparation of [Bmim]Br / AlBr 3 : Step 1 {[Bmim]Br}: Weigh 64.12g (0.78mol) of 1-methylimidazole into a 500ml three-necked flask, and stir rapidly at a constant temperature of 70°C. Slowly add 117.87 g (0.858 mol) of n-bromobutane dropwise into the three-necked flask with a constant pressure dropping funnel for 1 h. After the dropwise addition, the mixture was refluxed at 70° C. for 10 h. After the reaction was completed, cool to room temperature to obtain the crude product [Bmim]Br, which was transferred to a separatory funnel, washed (3 times) with 30ml ethyl acetate, and then the product was rotary evaporated at 60°C for 30min to remove residual ethyl acetate. ester. The remaining product was transferred to a beaker and placed in a vacuum drying oven at a temperature of 65°C, and dried to constant weight to obtain the finished product of 1-methyl-3-n-butylimidazole bromide ([Bmim]Br). Step 2 {[Bmim]Br / AlBr 3}: Weigh 50g of prepared [bmim]Br into a 250ml single-nec...

Embodiment 2

[0031] Preparation of Fe 3 o 4 @Zn-ZIF-8: Weigh 1.77g of zinc nitrate hexahydrate and dissolve it in 60.5ml of anhydrous methanol to obtain solution 1; weigh 9.85g of 2-methylimidazole and dissolve it in 60.5ml of anhydrous methanol to obtain a solution 2; After mixing solution 1 with solution 2, add 0.08g Fe 3 o 4 Disperse into the mixed liquid, stir magnetically at 50°C for 4h; after the reaction, centrifuge at 8000r.p.m, and wash with methanol three times; the obtained solid is vacuum-dried at 80°C overnight, and ground to obtain Fe3O4@Zn-ZIF-8 . like figure 2 Shown is Fe3O4@Zn-ZIF-8 obtained in the present invention. Example 3

Embodiment 3

[0032] Preparation of [Bmim]Br / AlBr3-Fe 3 o 4 @Zn-ZIF-8: Dissolve 0.4g of ionic liquid [Bmim]Br / AlBr3 in 5ml of anhydrous methanol, and weigh 0.63g of Fe 3 o 4 @ZIF-8 added [Bmim]Br / AlBr 3 After ultrasonic treatment for 10 minutes, seal it with plastic wrap and place it in a ventilated place for immersion for 24 hours, then separate the catalyst with a magnet, dry it in a vacuum oven at 80°C overnight, and place the solid catalyst in a muffle furnace for calcination at 220°C After grinding, the recyclable MOFs immobilized ionic liquid catalyst [Bmim]Br / AlBr3-Fe3O4@Zn-ZIF-8 was obtained. like image 3 Shown is [Bmim]Br / AlBr3-Fe3O4@Zn-ZIF-8 obtained in the present invention.

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 provides a catalyst for synthesizing salicylic acid by carboxylation of phenol and a preparation method thereof. The catalyst is a novel recyclable MOFs immobilized ionic liquid catalyst. The catalytically active component is a Lewis acidic ionic liquid, and the carrier is a magnetic core-shell MOFs nanocomposite Fe 3 o 4 @ZIFs. The method starts with a one-pot method in the magnetic Fe 3 o 4 Magnetic core-shell composite support (Fe 3 o 4 @ZIFs), and then synthesized an ionic liquid catalyst with Lewis acid active sites by a two-step method, using the impregnation method on Fe 3 o 4 Ionic liquid catalysts with Lewis acid active sites supported on the surface of @ZIFs. The catalyst has good catalytic performance for the reaction of phenol carboxylation to prepare salicylic acid. With the help of the external magnetic field effect, the catalyst has strong recyclability, and it still maintains high catalytic activity after recycling, and the selectivity of the product is high, and the process is green. Environmentally friendly, it is a new type of green chemical catalytic material with industrial application prospects.

Description

technical field [0001] The invention belongs to the field of salicylic acid synthesis, and in particular relates to a catalyst for synthesizing salicylic acid by phenol carboxylation and a preparation method. Background technique [0002] Salicylic acid (Salicylic Acid), also known as o-hydroxybenzoic acid. As an important pharmaceutical synthesis intermediate, its industrial synthesis is mainly based on the Kolbe-Schmitt reaction. This is a way to use CO 2 The industrial synthesis method as a reactant, that is, the process of introducing a carboxyl group on an aromatic ring through an electrophilic substitution reaction between carbon dioxide and phenol. It is divided into gas-solid phase reaction and gas-liquid phase reaction, and the method widely used in industry is the former. The method uses phenol as a raw material, undergoes an acid-base neutralization reaction with sodium hydroxide to generate sodium phenate, and then introduces carbon dioxide under a certain pre...

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): B01J31/22C07C51/15C07C65/10H01F1/113
CPCB01J31/1691C07C51/15H01F1/113B01J2531/26C07C65/10Y02P20/54Y02P20/584
Inventor 李乃旭石闻卿周建成陈聪阚道琴王楠王可
Owner SOUTHEAST UNIV
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