Thermosensitive type organic/inorganic hybrid dendrimers and preparation method thereof
A dendritic and macromolecular technology, applied in the field of organic/inorganic hybrid dendritic macromolecules and their preparation, to achieve the effect of reducing the difficulty of synthesis
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Embodiment 1
[0034] The present invention relates to POSS 8 -EtG 1 Preparation and synthesis. Synthetic route reference Figure 1-3 .
[0035] 1.1 The core point is a first-generation ethoxyether dendron with pentafluorophenol active ester ( 1b ) Synthesis
[0036] A first-generation ethoxyether dendron with the core point as a carboxyl group 1a (2.30 g, 3.50 mmol, refer to literature Li, W.; Zhang, A.; Schlüter, A. D. Chem. Commun. 2008 , 5523 and Yan J T; Li W; Liu K; Wu D L; Chen F; WuP Y; Zhang A. Chem. Asian J. 2011, 6, 3260 synthesis) and pentafluorophenol (0.97 g, 5.3 mmol) dissolved in 30 mL of dry dichloromethane and at -15 o C was stirred for 10 min, then 1-ethyl-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.81 g, 4.23 mmol) was added to the solution. The mixed solution was stirred at room temperature for 12 h, washed with saturated sodium bicarbonate solution and saturated brine, and the organic phase was dried with anhydrous magnesium sulfate and filtered. The...
Embodiment 2
[0042] The present invention relates to POSS 8 -EtG 2 Preparation and synthesis. Synthetic route reference Figure 1-3 .
[0043] 2.1 The core point is the diethoxyether branching unit of pentafluorophenol active ester ( 2b ) Synthesis
[0044] Diethoxyether dendron with the core point as carboxyl group 2a (2 g, 0.84 mmol, refer to literature Li, W.; Zhang, A.; Schlüter, A. D. Chem. Commun. 2008 , 5523 and Yan J T; Li W; Liu K; Wu D L; Chen F; WuP Y; Zhang A. Chem. Asian J. 2011, 6, 3260 synthesized) and pentafluorophenol (0.24 g, 1.30 mmol) dissolved in 20 mL of dry dichloromethane and at -15 o C was stirred for 10 min, then 1-ethyl-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.20 g, 0.98 mmol) was added to the solution. The mixed solution was stirred at room temperature for 12 h, washed with saturated sodium bicarbonate solution and saturated brine, and the organic phase was dried with anhydrous magnesium sulfate and filtered. The filtrate was concentrated ...
Embodiment 3
[0049] The synthetic route reference of the present invention Figure 9 .
[0050] Synthesis of dendrons with double bonds at the nucleus: Add 1 to 1.5 mmol of acryloyl chloride in dry dichloromethane (10 mL) dropwise to a solution of 1 mmol of benzyl alcohol at the nucleus ( 1a ) or second generation ( 2a ) ethoxyether dendrons, triethylamine (3~4.5 mmol) and DMAP (0.3~0.45 mmol) in dry DCM (100 mL) solution, keep the ice bath temperature at 0 during the dropwise addition oC After half an hour, the ice bath was removed, and stirring was continued at room temperature for 4 h, and then methanol was added dropwise to terminate the reaction. The reaction solution was sequentially washed with saturated NaHCO 3 solution and saturated NaCl solution, and after separation, use anhydrous MgSO 4 The organic phase is dried and filtered. Repurify with silica gel column chromatography, developing solvent is DCM / MeOH (30:1, v / v), obtains colorless oil ( 1b or 2b ).
[0051] Take 0....
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