Synthesis method of 2,2,6,6-tetramethylpiperidone with set end point judgment method

A technology of tetramethylpiperidone and synthesis method, applied in the direction of organic chemistry, etc., to achieve the effects of reducing the amount of by-products, simple post-processing, and mild conditions

Active Publication Date: 2021-07-30
YANTAI XINXIU CHEM TECH CO LTD +1
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The by-product cannot be converted into the target product 2,2,6,6-tetramethylpiperidone under the reaction conditions

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 2,2,6,6-tetramethylpiperidone with set end point judgment method
  • Synthesis method of 2,2,6,6-tetramethylpiperidone with set end point judgment method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] Embodiment 1, add acetone 87g (1.5mol), 8g (0.1mol) ammonium nitrate in the autoclave of 250mL; Pass into liquid ammonia 8.5g (0.5mol), heat up to 60 ℃ under stirring; Continuous detection in the reaction process When the pH value of the reaction system does not change within 30 minutes, the heating can be stopped, thereby terminating the reaction. At this time, the reaction time is about 4 hours, and the pressure of the autoclave is about 0.1 MPa; the concentration of the product in the GC is 48%.

[0024] After the reaction is completed, the reaction solution is suction-filtered in a Buchner funnel first, and the obtained filtrate is roughly steamed under normal pressure, and the obtained light components are recovered and used mechanically (that is, acetone is recovered by distillation); Sodium hydroxide is used to absorb the water generated by the reaction. The mass ratio of sodium hydroxide to the crude steamed heavy component (that is, the distillation substrate) ...

Embodiment 2

[0025] Embodiment 2, the reaction temperature of embodiment 1 is changed from 60 ℃ to 65 ℃, and the rest are equal to embodiment 1.

[0026] The final yield of 2,2,6,6-tetramethylpiperidone was 81.8%.

Embodiment 3

[0027] Embodiment 3, change the consumption of raw material into: acetone 87g (1.5mol), 4g (0.05mol) ammonium nitrate; Feed liquid ammonia 8.5g (0.5mol), all the other are equal to embodiment 1.

[0028] The final yield of 2,2,6,6-tetramethylpiperidone was 80.5%.

[0029] Embodiment 3, change the consumption of raw material into: acetone 87g (1.5mol), 12g (0.15mol) ammonium nitrate; Feed liquid ammonia 8.5g (0.5mol), all the other are equal to embodiment 1.

[0030] The final yield of 2,2,6,6-tetramethylpiperidone was 81.8%.

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 method for synthesizing 2,2,6,6-tetramethylpiperidone with an end-point determination method. The synthesis reaction is as follows: acetone and ammonia are used as raw materials and heated under the action of ammonium nitrate as a catalyst Reaction; after the reaction is over, acetone is recovered by distillation, and the distillation substrate is washed with alkali and then rectified to obtain 2,2,6,6-tetramethylpiperidone; during the reaction, the pH value is detected, and within 30 minutes If the pH value remains unchanged, it is determined that the end of the reaction has been reached, and the heating is stopped to end the above reaction. The synthesis method of the invention has mild conditions, cheap and easy-to-obtain raw materials and catalysts, fewer side reactions, and the reduction in the amount of by-products makes post-processing simpler and higher yield.

Description

technical field [0001] The invention relates to a synthesis method of 2,2,6,6-tetramethylpiperidone with an end point judgment mode set. Background technique [0002] 2,2,6,6-Tetramethylpiperidone, which has the formula C 9 h 17 NO, the structural formula is as follows: [0003] [0004] The secondary amine group of 2,2,6,6-tetramethylpiperidone can be converted into a stable nitroxide free radical under thermal and photooxidative conditions, which can effectively free the alkoxylate in the polymer 2,2,6,6-Tetramethylpiperidone is an important raw material for the preparation of hindered amine light stabilizers . At present, in literature reports, the method for producing 2,2,6,6-tetramethylpiperidone mainly contains the following: [0005] Method 1: Using acetone and liquid ammonia as raw materials, first generate acetonin, diacetone alcohol or phorone, separate and purify acetonin, diacetone alcohol or phorone, and then pass ammonia gas to generate 2,2,6 ,6-Tetram...

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): C07D211/74C07D211/02
CPCC07D211/02C07D211/74
Inventor 史雅静王轲钱超张秀秀
Owner YANTAI XINXIU CHEM TECH CO LTD
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