Functionalized hyperbranched polyphenylene ether and method for preparing same
A polyphenylene ether and functionalization technology, applied in the field of hyperbranched polymer and its preparation, modified hyperbranched polyphenylene ether and its preparation, can solve problems such as unreported technology, and achieve the expansion of compatibility and reaction performance, and the effect of expanding application scale
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0023] (1) Synthesis of hyperbranched polyphenylene ether
[0024] Under a nitrogen atmosphere, 2.41g (6.82mmol) of 4-bromo-4', 4"-dihydroxytriphenylmethane, 1.08g (7.81mmol) of anhydrous K 2 CO 3 and 25.0ml toluene were sequentially added to 98ml dimethyl sulfoxide (DMSO), and the temperature was raised to reflux for dehydration for 3 hours. Afterwards, the temperature of the reaction system was lowered to 45° C., 13.5 mg (0.14 mmol) of catalyst CuCl was added, and then the temperature was raised to 170° C. and reacted at a constant temperature for 40 hours. After the reaction, the mixture was cooled to room temperature, acidified with hydrochloric acid, stirred for 0.5 hours, dropped into methanol / water mixture (volume ratio 4 / 6) to precipitate, filtered, and vacuum-dried at 60°C to obtain a crude product. The crude product was dissolved in a small amount of tetrahydrofuran (THF) and filtered; the filtrate was precipitated with cyclohexane, filtered and washed with cyclohe...
Embodiment 2
[0036] Preparation of Functionalized Hyperbranched Polyphenylene Ether
[0037]Under an argon atmosphere, at normal temperature, the hyperbranched polyphenylene ether, 10g of potassium hydroxide, 100g of dimethylformamide (DMF) and 1g of tetrabutyl bromide prepared in the first step (1) of the 100g embodiment Ammonium was put into a three-necked flask. Raise the temperature to 70°C and stir for 1 hour. After cooling down to 40°C, start to add 20g of 3-bromopropene dropwise, and finish dropping in 0.7 hours; then raise the temperature to 60°C, keep warm and reflux for 3 hours, then raise the temperature to 80°C, keep warm and reflux for 3 hours. After the reaction was completed, it was cooled to room temperature, stirred and dropped into a mixed solution of methanol and water (volume ratio 1:3), and filtered. After the filter cake is vacuum-dried at 50°C, it is dissolved in tetrahydrofuran, dropped into cyclohexane while stirring, filtered, and the filter cake is vacuum-dried...
Embodiment 3
[0040] Preparation of Functionalized Hyperbranched Polyphenylene Ether
[0041] Under a nitrogen atmosphere, at normal temperature, the hyperbranched polyphenylene ether, 15g sodium hydroxide, 250g dimethylacetamide (DMAc) and 2g benzyltriethyl chloride prepared in step (1) of 100g embodiment Ammonium was put into a three-necked flask. Raise the temperature to 60°C and stir for 0.5 hours. After cooling down to 50°C, 30 g of 3-chloropropene was added dropwise, and the dropwise was completed within 2.5 hours. Then the temperature was raised to 60°C, and the temperature was kept at reflux for 4 hours, and then the temperature was raised to 80°C, and the temperature was kept at reflux for 3 hours. After the reaction was completed, it was cooled to room temperature, stirred and dropped into a mixed solution of methanol and water (volume ratio 1:2), and filtered. After the filter cake was vacuum dried at 60°C, it was dissolved in tetrahydrofuran, dropped into cyclohexane while st...
PUM
Property | Measurement | Unit |
---|---|---|
hydroxyl value | aaaaa | aaaaa |
hydroxyl value | aaaaa | aaaaa |
Branching factor | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com