Benzoate-based burning rate catalyst containing dinuclear ferrocene group and preparation method of benzoate-based burning rate catalyst
A burning rate catalyst, ferrocene-based technology, applied in chemical instruments and methods, metallocene, organic chemistry, etc., can solve problems such as complex synthesis process, achieve simple operation, good thermal stability, and improve thermal stability. Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Example Embodiment
[0024] Example 1
[0025] Prepare bis-(ferrocenylmethyl-1,2,3-triazolylmethyl) terephthalate with the following structural formula
[0026]
[0027] Add 0.2230g (1mmol) di-2-ynyl propyl terephthalate and 0.4931g (2.05mmol) azidomethylferrocene into a 250mL round bottom flask. 2 Add 30 mL of methanol under the atmosphere and stir evenly, then add dropwise 15 mL of an aqueous solution containing 0.077 g (0.3 mmol) of copper sulfate pentahydrate and 15 mL of an aqueous solution containing 0.0604 g (0.3 mmol) of sodium ascorbate, stirring at room temperature for 24 hours, and filtering to obtain the crude product. The crude product was separated by column chromatography to obtain bis-(ferrocenylmethyl-1,2,3-triazolylmethyl) terephthalate, the yield was 82%, and the structural characterization data were: FT-IR(cm -1 ):3431m,3155m,2955w,1715vs,1626m,1383m,1335m,1265vs,1106vs,1044m,933m,801s,718m,490s; 1 H NMR(400MHz, CDCl 3 ): δ8.04(s, 4H), 7.59(s, 2H), 5.43(s, 4H), 5.30(s, 4H), 4.29(s, ...
Example Embodiment
[0028] Example 2
[0029] Preparation of phthalic acid bis-(ferrocenyl methyl-123-triazolyl methyl) ester with the following structural formula
[0030]
[0031] In this example, the di-2-ynyl propyl terephthalate in Example 1 is replaced with equimolar di-2-ynyl propyl phthalate. The other steps are the same as in Example 1. The yield of bis-(ferrocenylmethyl-1,2,3-triazolylmethyl) formate is 79%. The structural characterization data is: FT-IR(cm -1 ): 3427m, 3094m, 2955w, 1723vs, 1626w, 1445m, 1383m, 1272vs, 1120vs, 1058s, 940m, 822s, 753m, 635w, 490s; 1 H NMR(400MHz, CDCl 3 ): δ7.68 (s, 2H), 7.62 (s, 2H), 7.51 (s, 2H), 5.30 (s, 8H), 4.31 (s, 4H), 4.19 (s, 14H).
PUM
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.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap