Compound containing spiro-dimethyl anthracene fluorene and application of compound
A technology of dimethyl anthracene fluorene and compound, which can be used in organic chemistry, chemical instruments and methods, electrical components, etc., and can solve different problems.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0096] Embodiment 1: the synthesis of compound 8:
[0097]
[0098] In a 250ml three-neck flask, under the protection of nitrogen, add 0.01mol raw material A1, 0.012mol raw material B1, 150ml toluene and stir to mix, then add 0.03mol sodium tert-butoxide, 5×10 -5 molPd 2 (dba) 3 , 5×10 -5 mol of tri-tert-butylphosphine, heated to 105°C, refluxed for 24 hours, sampling plate, showed no remaining bromide, the reaction was complete; naturally cooled to room temperature, filtered, and the filtrate was rotary evaporated under reduced pressure (-0.09MPa, 85°C ), through a neutral silica gel column, to obtain the target product, HPLC purity 99.3%, yield 84.7%;
[0099] Elemental analysis structure (molecular formula C 52 h 36 N 2 ): theoretical value C, 90.67; H, 5.27; N, 4.07; test value: C, 90.67; H, 5.28; N, 4.05. ESI-MS(m / z)(M + ): The theoretical value is 688.29, and the measured value is 688.68.
Embodiment 2
[0100] Embodiment 2: the synthesis of compound 15:
[0101]
[0102] In a 250ml three-necked flask, under the protection of nitrogen, add 0.01mol raw material A1, 0.012mol raw material B2, 150ml toluene and stir to mix, then add 0.03mol sodium tert-butoxide, 5×10 -5 molPd 2 (dba) 3 , 5×10 -5 mol of tri-tert-butylphosphine, heated to 105°C, refluxed for 24 hours, sampling plate, showed no remaining bromide, the reaction was complete; naturally cooled to room temperature, filtered, and the filtrate was rotary evaporated under reduced pressure (-0.09MPa, 85°C ), through a neutral silica gel column, to obtain the target product, HPLC purity 99.5%, yield 82.9%;
[0103] Elemental analysis structure (molecular formula C 49 h 37 N): theoretical value C, 91.98; H, 5.83; N, 2.19; test value: C, 92.00; H, 5.82; N, 2.18. ESI-MS(m / z)(M + ): The theoretical value is 639.29, and the measured value is 639.71.
Embodiment 3
[0104] Embodiment 3: the synthesis of compound 16:
[0105]
[0106] The preparation method of compound 16 is the same as that in Example 1, except that raw material B1 is replaced with raw material B3.
[0107] Elemental analysis structure (molecular formula C 52 h 36 N 2 ): theoretical value C, 90.67; H, 5.27; N, 4.07; test value: C, 90.67; H, 5.28; N, 4.05. ESI-MS(m / z)(M + ): The theoretical value is 688.29, and the measured value is 688.65.
PUM
Property | Measurement | Unit |
---|---|---|
Thickness | aaaaa | aaaaa |
Thickness | aaaaa | aaaaa |
Thickness | 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