A kind of anti-ultraviolet flame retardant epoxy resin curing agent and preparation thereof
An epoxy resin curing and flame retardant technology, which is applied in organic chemistry, chemical instruments and methods, compounds of Group 5/15 elements of the periodic table, etc., can solve the problems of flammability, easy aging, etc. Effects of UV and flame retardant properties
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0021] The preparation of embodiment 1 p-nitrocinnamic acid
[0022] Weigh 15g of p-nitrobenzaldehyde and 6g of sodium acetate into the reaction flask, add 30mL of acetic anhydride, reflux at 180°C for 8h, after the reaction, add 50mL of water, dissolve with saturated potassium carbonate and adjust the pH to 8, decolorize with activated carbon, filter while hot , adjust the pH to about 4 with hydrochloric acid, filter, and get it.
[0023] ES: M / Z 181[M+H] + .
Embodiment 2
[0024] Example 2: Preparation of p-nitrocinnamoyl chloride
[0025] Weigh 5 g of p-nitrocinnamic acid obtained in Example 1 into a reaction flask, add 30 mL of thionyl chloride and 2 mL of DMF, heat under reflux for 2 h, evaporate the solvent under reduced pressure, and use it directly in the next step.
Embodiment 3
[0026] Example 3: Preparation of 2-hydroxy-4-(2-p-nitrophenylacrylate) benzophenone
[0027] Weigh 3.4 g of 2,4-dihydroxybenzophenone into a reaction flask, add 3 mL of triethylamine, 20 mL of tetrahydrofuran, and slowly dropwise add 10 mL of the tetrahydrofuran solution dissolved in the result of Example 2 at 0-5 °C, and the dripping is completed. , continue to stir at 0-10 ℃ for 4 h, after the reaction, add 30 mL of water, extract with dichloromethane (3*50 mL), dry with anhydrous sodium sulfate, and purify by column chromatography to obtain the title compound.
[0028] ES: M / Z 390[M+H] + .
[0029] 1 H NMR (600MHz, CDCl 3 )(δ,ppm): 8.51~8.50(m,2H), 8.02~8.00(m,2H), 7.82~7.81(m,2H), 7.55~7.53(m,2H), 7.40~7.39(m,2H) ), 6.98~6.95(m, 2H), 6.50(s, 1H), 6.37(s, 1H), 5.00(s, 1H).
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


