Method for preparing alkoxyl silicone oligomer
An organosilicon oligomer and alkoxy technology, which is applied in the field of organosilicon material synthesis, can solve the problems of personnel safety threats, cumbersome neutralization processing operations, complicated reaction processes, etc., and achieves a stable and easy-to-control reaction process and moderate reactivity. , the effect of chemical stability
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Embodiment 1
[0041] Rectify to separate the oligomerization mixture components in the organosilicon by-products, take 500g and put it into a reaction kettle with a rectifying column, then add 500g of toluene, after stirring evenly, add 400g dropwise at 40°C and stirring speed of 400r / min Put methyl ether into the reaction kettle, the generated HCl is absorbed and used to prepare hydrochloric acid solution. After the dropwise addition, it is equilibrated for 5 hours, cooled to 30°C, under 140mmHg, desorbed HCl for 2h, and then heated at a speed of 15°C / h from 40°C Gradually rise to 70°C, and under reduced pressure (under 140mmHg), separate the low-boiling components in the reacted mixed solution through a rectifying column until no liquid is separated, and then add 1g of sodium bicarbonate to the mixed solution , continuously stirred for 30 min, and filtered to obtain a clear neutral alkoxy-substituted organosilicon oligomer, and the product yield can reach 85%.
Embodiment 2
[0043] The oligomer components in the organic silicon by-products were separated by rectification, and 500g was put into a reaction kettle with a rectification column, and then 1000g of cyclohexane was added. After stirring evenly, at 55°C and a stirring speed of 600r / min, Add 600g of diethyl ether to the reaction kettle, the generated HCl is absorbed and used to prepare hydrochloric acid solution, after the dropwise addition is completed, equilibrate for 3h, cool to 25°C, desorb HCl for 1.5h at 100mmHg, and then heat at a speed of 15°C / h Gradually rise from 40°C to 70°C, and under reduced pressure (100mmHg), separate the low-boiling components in the reaction mixture through a rectification column until no liquid is separated, and then add 2g of carbonic acid to the mixture Potassium hydrogen, continuously stirred for 45 minutes, and filtered to obtain a clear neutral alkoxy-substituted organosilicon oligomer, and the product yield can reach 89%.
Embodiment 3
[0045]The oligomer components in the organic silicon by-products were separated by rectification, and 500g was put into a reaction kettle with a rectification column, and then 500g of cyclopentane was added. Add 200g of methanol to the reaction kettle, the generated HCl is absorbed and used to prepare hydrochloric acid solution, after the dropwise addition is completed, equilibrate for 1h, cool to 20°C, and desorb HCl for 1h at 70mmHg, then heat at a speed of 15°C / h by 40 ℃ gradually rises to 70 ℃, under reduced pressure (under 70mmHg), the low-boiling components in the reaction mixed solution are separated through a rectification column until no liquid is separated, and then 2.5g of hydrogen carbonate is added to the mixed solution ammonium, continuously stirred for 60 min, and filtered to obtain a clear neutral alkoxy-substituted organosilicon oligomer, and the product yield can reach 92%.
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