2504-64-5Relevant articles and documents
Fritz,Huber
, p. 163,164,172 (1976)
Process for Preparing Polysilylalkane
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Paragraph 0056-0057; 0080-0082, (2020/04/17)
Polysilylalkane according to the present invention is represented by following formula. The present invention has an advantage that bis(silyl)alkanes or tri(silyl)alkanes can be manufactured in a high yield by dehydrochlorination with a small amount of catalyst by using a silane compound having a dichloro organic matter or a dichloromethyl group.COPYRIGHT KIPO 2020
Process for Preparing Polysilylalkane
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Paragraph 0071-0073, (2016/11/02)
According to the present invention, polysilylalkane is represented by chemical formula 3. In chemical formula 3, m is equal to n, and n is equal to zero; and R^3 is a chloromethyl group. In the case of R^4 is H, -SiMe_2Cl, -SiMe_3, -SiMeCl_2, and -SiCl_3, R^3 is equal to -SiCl_3. In the case of R^4 is H, and R^5 is equal to R^6 and R^6 is equal to Me, or R^5 is equal to Me and R^6 is equal to Et, R^3 is -SiCl_3. In the case of R^4 is H, R^5 is equal to -CH_2SiCl_3, and R^6 is Me, R^3 is equal to -SiCl_3. In the case of R^4 is H, R^5 is equal to R^6 and R^6 is equal to -CH_2SiCl_3, R^3 is equal to Et, SiMe_2Cl, -SiMeCl_2, and -SiCl_3, and m is an integer of zero to nine. The manufacturing method is capable of manufacturing bis(silyl)alkane or tri(silyl)alkane in a high yield with a small amount of a catalyst.COPYRIGHT KIPO 2016
Multifunctional thiols from the highly selective reaction of mercaptoalcohols with chlorosilanes
Jennings, Abby R.,Son, David Y.
, p. 3467 - 3469 (2013/06/04)
Multifunctional thiols were synthesized by the selective reaction of chlorosilanes with mercaptoalcohols. Reaction of the mercaptoalcohols through the thiol group was not observed. Utilizing this method, thiols of varying structural diversity were prepared.