Organic base catalyst and method for catalyzing alcoholysis of polycaprolactone by using organic base catalyst
A polycaprolactone and organic base technology, applied in organic compound/hydride/coordination complex catalysts, organic chemistry, chemical instruments and methods, etc., can solve the problem of high temperature, metal residue, long reaction time, etc. problem, achieve the effect of reducing energy loss, saving cost and shortening production cycle
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Embodiment 1
[0028] The reaction process of the present embodiment is as follows:
[0029]
[0030] The specific operation process of this embodiment is as follows:
[0031] Take a 25mL Schlenk bottle, bake it and replace the argon gas, add 1.14g polyε-caprolactone (M n =10.7kg / mol, ), then added 13.9 mg of TBD catalyst, 10 mL of toluene solvent, 5 mL of methanol was added outside the glove box, and the reaction was stirred at 80 °C. After the reaction for 2 h, the reaction system was detected by nuclear magnetic resonance. The conversion rate of the polymer was 92%. - Methyl hydroxycaproate.
[0032] Among them, TBD is
Embodiment 2
[0034] The reaction process of the present embodiment is as follows:
[0035]
[0036] The specific operation process of this embodiment is as follows:
[0037] Take a 25mL Schlenk bottle, bake it and replace the argon gas, add 1.14g polyε-caprolactone (M n =10.7kg / mol, ), then 13.9 mg of TBD catalyst was added, 5 mL of methanol was added outside the glove box, and the reaction was stirred at 80 °C. After the reaction for 0.5 h, the reaction system was detected by nuclear magnetic resonance. The conversion rate of the polymer was 93%, and the obtained product was 6-hydroxyhexane methyl acid. figure 1 To obtain methyl 6-hydroxyhexanoate 1 H NMR nuclear magnetic spectrum.
Embodiment 3
[0039] The reaction process of the present embodiment is as follows:
[0040]
[0041] The specific operation process of this embodiment is as follows:
[0042] Take a 25mL Schlenk bottle, bake it and replace the argon gas, add 1.14g polyε-caprolactone (M n =10.7kg / mol, ), then 11.75 mg of t-BuP was added 1 Catalyst, 10 mL of toluene solvent, 5 mL of methanol was added outside the glove box, and the reaction was stirred at 80 °C. After 5 hours of reaction, the reaction system was detected by nuclear magnetic resonance. The conversion rate of the polymer was 94%, and the obtained product was methyl 6-hydroxyhexanoate.
[0043] Among them, t-BuP 1 for where R is methyl.
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