Polyurethane composition, preparation method and application thereof
A polyurethane and composition technology, applied in the field of polyurethane composition and its preparation, can solve problems such as loss, no reaction sites of flame retardants, and environmental pollution
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preparation example 1
[0085] A phosphorus-containing small molecular alcohol has the following structure:
[0086]
[0087] The preparation method is as follows:
[0088]Add 2 mol of dimethyl phosphite, 1 mol of o-phthalaldehyde, and 20 mL of ethanol into a three-necked flask equipped with magnetic stirring and a thermometer. Under stirring, keep the temperature below 5°C in an ice-water bath, add 2 mol of triethylamine dropwise, gradually Raise the temperature to reflux, continue the reaction for 1 h, and distill under reduced pressure to obtain the reactive flame retardant with the above structure.
[0089] 1 H NMR (400MHz, DMSO-d6): δ=7.10-7.14(s, 4H, ph-H), 4.58-4.62(s, 2H, -CH-P), 3.40-3.45(d, 12H, -P-O- CH 3 ).
preparation example 2
[0091] A phosphorus-containing small molecular alcohol has the following structure:
[0092]
[0093] The preparation method is as follows:
[0094] Add 1 mol of trimethyl phosphate, 2.1 mol of 1,4-benzenediethanol, 0.05 mol of cadmium acetate and 0.05 mol of antimony trioxide into a 200mL three-port glass reactor, heat up to reflux temperature, reflux for 7 hours, filter after cooling, spin Methanol was evaporated to give the product.
[0095] 1 H NMR (400MHz, DMSO-d6): δ=7.02-7.16(m,8H,-Ph),4.29-4.41(m,4H,-P-O-C H 2 -),4.00-4.04(t,2H,-OH),3.73-3.85(m,4H,-C H 2 -OH),3.44-3.48(d,3H,-P-O-CH 3 ),2.92-2.96(m,4H,-P-O-CH 2 -C H 2 -),2.73-2.83(m,4H,-C H 2 -CH 2 -OH).
preparation example 3
[0097] A phosphorus-containing small molecular alcohol has the following structure:
[0098]
[0099] The preparation method is as follows:
[0100] Add 1 mol of triphenyl phosphate, 2.1 mol of 1,4-benzenediethanol, 0.05 mol of cadmium acetate and 0.05 mol of antimony trioxide into a 200mL three-port glass reactor, heat up to reflux temperature, reflux for 10 hours, filter after cooling, reduce The benzyl alcohol was removed by distillation to obtain the product.
[0101] 1 H NMR (400MHz, DMSO-d6): δ=7.03-7.28(m,13H,-Ph),4.30-4.40(m,4H,-P-O-C H 2 -),4.23-4.26(t,2H,-OH),3.76-3.87(m,4H,-C H 2 -OH),2.93-2.97(m,4H,-P-O-CH 2 -C H 2 -),2.76-2.84(m,4H,-C H 2 -CH 2 -OH).
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