27804-64-4Relevant articles and documents
Method for manufacturing of alkylaminosilane compound
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Paragraph 0087-0089, (2021/04/29)
The present invention relates to a method for preparing alkylaminosilane compounds capable of obtaining high purity alkylaminosilane compounds in high yield.
Synthesis method of bis(diethylamino)silane
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Paragraph 0015-0026, (2018/08/04)
The invention provides a synthesis method of bis(diethylamino)silane. The method is characterized by comprising the following steps of adding 100 parts of dichlorosilane, 1000 to 2000 parts of hexaneand 5 to 20 parts of white clay catalysts into a reactor in parts by weight; introducing nitrogen gas; dripping 300 to 600 parts of diethylamine under the stirring condition for reaction; maintainingthe temperature of the reaction system at 40 to 60 DEG C; after the dripping completion, performing heat insulation for 5 to 10 hours; then, obtaining the bis(diethylamino)silane by the existing impurity removal technology in industry.
Preparation method of di(diethylamino)silane
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Paragraph 0019; 0020, (2017/01/02)
The invention provides a preparation method of di(diethylamino)silane. The method comprises the following steps: step 1, adding an alkane CnH(2n+2) (n>=5) solution of n-butyllithium into a reactor protected by inert atmosphere, dropwise adding diethylamine for a reaction while performing stirring, maintaining the temperature of the reaction system in a range from -60 DEG C to -30 DEG C, and performing stirring for reaction for 10-15 h; step 2, pumping dichlorosilane in at a temperature in a range from -60 DEG C to -30 DEG C, performing stirring for reaction for 15-20 h while maintaining the temperature in a range from -60 DEG C to -30 DEG C, increasing the temperature to a room temperature, and evaporating alkane CnH(2n+2) (n>=5) under a normal pressure; and step 3, performing vacuum distillation to make a coarse di(diethylamino)silane product out. The coarse di(diethylamino)silane product is subjected to vacuum distillation to obtain di(diethylamino)silane with high purity. The preparation method has the beneficial effects that the selected reagents are free of toxicity, thereby ensuring safety of operators; the reaction process is relatively mild and has no potential safety hazard; and the reaction efficiency is very high.