1789-58-8Relevant articles and documents
Direct synthesis of organochlorosilanes by the reaction of metallic silicon with hydrogen chloride and alkene/alkyne
Okamoto, Masaki,Onodera, Satoshi,Yamamoto, Yuji,Suzuki, Eiichi,Ono, Yoshio
, p. 1275 - 1276 (1998)
Organosilicon compounds were directly synthesized from metallic silicon, alkene/alkyne and HCl, EtHSiCl2 being obtained with 47% selectivity from Si, C2H4 and HCl at 513 K, and CH2=CHSiHCl2 and EtHSiC
SYNTHESIS OF ORGANO CHLOROSILANES FROM ORGANOSILANES
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Page/Page column 38, (2019/04/16)
The invention relates to a process for the production of chlorosilanes by subjecting one or more hydndosilanes to the reaction with hydrogen chloride in the presence of at least one ether compound, and a process for the production of such hydndosilanes serving as starting materials.
Lewis Base Catalyzed Selective Chlorination of Monosilanes
Sturm, Alexander G.,Schweizer, Julia I.,Meyer, Lioba,Santowski, Tobias,Auner, Norbert,Holthausen, Max C.
supporting information, p. 17796 - 17801 (2018/11/23)
A preparatively facile, highly selective synthesis of bifunctional monosilanes R2SiHCl, RSiHCl2 and RSiH2Cl is reported. By chlorination of R2SiH2 and RSiH3 with concentrated HCl/ether solutions, the stepwise introduction of Si?Cl bonds is readily controlled by temperature and reaction time for a broad range of substrates. In a combined experimental and computational study, we establish a new mode of Si?H bond activation assisted by Lewis bases such as ethers, amines, phosphines, and chloride ions. Elucidation of the underlying reaction mechanisms shows that alcohol assistance through hydrogen-bond networks is equally efficient and selective. Remarkably, formation of alkoxysilanes or siloxanes is not observed under moderate reaction conditions.
A direct method for preparing ethyldichlorosilane and its comparison with known alternative methods
Lebedev,Sheludyakov,Lebedeva,Ovcharuk,Govorov,Kalinina
, p. 629 - 633 (2014/11/08)
Various methods, alternative to direct synthesis, for preparing an important commercial organosilicon monomer, ethyldichlorosilane, were studied in detail. The methods, including organomagnesium and organoaluminum procedures, hydrosilylation, and combined methods, were analyzed from the viewpoint of feasibility of laboratory and small-tonnage commercial production, and their advantages and drawbacks were revealed.
Direct synthesis of organodichlorosilanes by the reaction of metallic silicon, hydrogen chloride and alkene/alkyne and by the reaction of metallic silicon and alkyl chloride
Okamoto, Masaki,Onodera, Satoshi,Yamamoto, Yuji,Suzuki, Eiichi,Ono, Yoshio
, p. 71 - 78 (2007/10/03)
Dichloroethylsilane was synthesized by the reaction of metallic silicon, hydrogen chloride and ethylene using copper(I) chloride as the catalyst, the silicon conversion and the selectivity for dichloroethylsilane being 36 and 47%, respectively. At a lower reaction temperature or at a higher ratio of ethylene: hydrogen chloride a higher selectivity was obtained, however the silicon conversion was lower. The silicon-carbon bond formation is caused by the reaction of a surface silylene intermediate with ethylene. The reaction with propylene in place of ethylene gave dichloroisopropylsilane (22% selectivity) and dichloro-n-propyl-silane (8% selectivity) together with chlorosilanes. A part of the dichloroisopropylsilane is formed by the reaction of silicon, hydrogen chloride and isopropyl chloride formed by hydrochlorination of propylene. Use of acetylene instead of alkenes resulted in dichlorovinylsilane formation with a 34% selectivity. Alkyldichlorosilanes were also produced directly from silicon with alkyl chlorides, propyl and butyl chlorides. During the reaction the alkyl chloride is dehydrochlorinated over the surface of copper originating from the catalyst to afford hydrogen chloride and alkene. The hydrogen chloride formed participates in the formation of the silicon-hydrogen bond in alkyldichlorosilane, and the reaction of silicon, hydrogen chloride and alkene also causes alkyldichlorosilane formation. The reaction with isopropyl chloride gave a very high selectivity (85%) for dichloroisopropylsilane, the silicon conversion being 86%. The Royal Society of Chemistry 2001.
Process for preparing alkylhydrogenchlorosilanes
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, (2008/06/13)
Alkylhydrogenchlorosilanes of formula I: wherein R are identical or different alkyl radicals, x is 1 or 2 and y is 1 or 2 and the sum of x and y is equal to 3, are prepared by comproportionating alkylchlorosilanes of formula II: wherein R denotes identical or different alkyl radicals, a is 1 or 2 and n is 2 or 3 and the sum of a and n is equal to 4 with hydrogenchlorosilanes of formula III: wherein R denotes identical or different alkyl radicals, b is 0, 1, 2 or 3 and c is 1, 2, 3 or 4 and the sum of b and c is equal to or smaller than 4, in the presence of a catalyst saturated with a hydrogen halide.
SELECTIVE REDISTRIBUTION REACTIONS OF ORGANOSILANES IN THE PRESENCE OF CHLOROPLATINIC ACID
Benkeser, Robert A.,Yeh, Ming-Hsiung
, p. 239 - 244 (2007/10/02)
Tetrasubstituted silanes of the general formula R2SiR'2 undergo redistribution reactions quite selectively in the presence of SiHCl3 and chloroplatinic acid.It is the smallest and seemingly the least hindered of the R groups on the tetrasubstituted silane which exchange most readily with a chloro group on trichlorosilane.
