Tridemorph synthesis process
A synthesis process, the technology of tridemorpholine, applied in the direction of organic chemistry, can solve the problem of many by-products, achieve the effects of reducing corrosion intensity, mild reaction conditions, and changing the complexity of the process
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Embodiment 1
[0065] 500g tridecyl alcohol, 500g tridecane are added in the reactor;
[0066] Add 10g of catalysts (mixed by methyl copper, binuclear methyl nickel, dimethyl zinc and trimethyl aluminum in a weight ratio of 1:1:1:1) in the reactor, mix under stirring, Introduce hydrogen gas at a rate of 0.1L, and raise the temperature of the reactor to 230°C in about 2 hours;
[0067] When the temperature of the reactor rises to 230°C, start to slowly add 400g of 2,6-dimethylmorpholine dropwise, maintain the pressure in the reactor at 0.3Mpa, and the temperature at 230-240°C until the end of the reaction. Or intermittently water and unreacted 2,6-dimethylmorpholine are taken out from the top of the tower; during the reaction, the reaction sample is detected by GC, such as figure 1 As shown, peaks appear at retention times (min.) of 1.716, 1.838, 1.891, 2.014, 2.273, 2.357, 2.447, 2.530, 4.563, 9.237, 13.301, 13.379, wherein 1.716, 4.563, 9.237 correspond to 2,6 - Dimethylmorpholine (8.299%...
Embodiment 2
[0071] 500g tridecyl alcohol, 400g tridecane are added in the reactor;
[0072] Add 9g of the fresh catalyst used in Example 1 and 2g of the catalyst recovered from Example 1 in the reactor, mix under stirring, feed hydrogen, and heat up the reactor;
[0073] When the temperature of the reaction kettle rose to 225°C, slowly drop 400g of 2,6-dimethylmorpholine and 50g of 2,6-dimethylmorpholine recovered and purified by distillation in Example 1, and keep the reaction kettle The pressure is 0.35Mpa, and the temperature is 230-245°C until the end of the reaction; during the reaction, the reaction sample is detected by GC, such as image 3 As shown, peaks appear at the retention times (min.) of 1.717, 1.840, 1.891, 2.013, 2.061, 2.343, 2.444, 2.576, 2.767, 4.545, 6.983, 7.147, 7.261, 9.238, 13.272, wherein 1.717, 4.545, 9.238 corresponds to 2,6-dimethylmorpholine (7.414%), tridecane+tridecyl alcohol (45.986%), and tridecylmorpholine (45.947%), respectively.
[0074] After the dr...
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