Surface treated resin products
A resin product and surface treatment technology, applied in the field of resin products, can solve problems such as insufficient wear resistance, and achieve the effects of high water and oil repellency, specific adhesion, and excellent wear resistance
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[0294] Hereinafter, synthesis examples, examples, reference examples, and comparative examples are shown, and the present invention will be described in more detail, but the present invention is not limited by the following examples.
[0295] Examples and comparative examples used the compounds obtained in the following synthesis examples.
Synthetic example 1
[0296] [Synthesis Example 1] Synthesis of Compound 1
[0297] 150 g of tetrahydrofuran and 300 g of 1,3-bis(trifluoromethyl)benzene were mixed in a reaction vessel, and 160 ml of 0.7 M allylmagnesium bromide was added dropwise. Then, slowly drop into the following formula (A)
[0298] [Chemical 55]
[0299]
[0300] Represented compound 200g (4.8×10 -2 mol), heated at 60°C for 4 hours. After heating, it was cooled to room temperature, and the solution was dropped into 300 g of a 1.2M hydrochloric acid aqueous solution to stop the reaction. After recovering the fluorine compound layer as the lower layer by a liquid separation operation, it was washed with acetone. The fluorine compound layer as the lower layer after washing was recovered again, and the remaining solvent was distilled off under reduced pressure to obtain the following formula (B):
[0301] [Chemical 56]
[0302]
[0303] Denotes polymers containing fluoropolyether groups.
[0304] Put into by follow...
Synthetic example 2
[0331] [Synthesis Example 2] Synthesis of Compound 2
[0332] In a reaction vessel, 100 g of 1,3-bis(trifluoromethyl)benzene, 8.2 g of DBU (diazabicycloundecene) (5.4×10 -2 mol), by the following formula (B)
[0333] [Chemical 61]
[0334]
[0335] Represented compound 114g (2.7×10 -2 mol) after mixing, drop 5.8g (5.4×10 - 2 mol). Then, it heated at 50 degreeC for 3 hours. After heating, it was cooled to room temperature, and aqueous hydrochloric acid solution was added dropwise. The fluorine compound layer as the lower layer was recovered by a liquid separation operation, and washed with methanol. The fluorine compound layer as the lower layer after washing is recovered again, and the remaining solvent is distilled off under reduced pressure to obtain the following formula (E):
[0336] [chem 62]
[0337]
[0338] Denotes polymers containing fluoropolyether groups.
[0339] 1 H-NMR
[0340] δ0-0.2(-OSi(C H 3 ) 3 )9H
[0341] δ2.4-2.6(-C H 2 CH=CH 2 )4...
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