Methyldichlorosilane → (2-Trimethylsilylethyl)methyldichlorosilane

HRID 327376

Reaction equation

HRID 327376 reaction equation
[CH3:1][Si:2]([CH:5]=[CH2:6])([CH3:4])[CH3:3].[CH3:7][SiH:8]([Cl:10])[Cl:9]>[H+].[H+].Cl[Pt-2](Cl)(Cl)(Cl)(Cl)Cl.CCCCCC>[CH3:1][Si:2]([CH3:4])([CH3:3])[CH2:5][CH2:6][Si:8]([CH3:7])([Cl:10])[Cl:9]

Participants

5

Procedure

There was allowed 100 g (1.0 mmol) of trimethylsilyl ethene to react with 127 g (1.1 mol) of methyldichlorosilane in a 500-ml flask equipped with a dropping funnel, reflux condenser, stirrer and nitrogen gas introducing tube, by steps of placing 20 ml of a mixture of trimethylsilyl ethene and methyldichlorosilane and 0.0051 g (0.01 mmol) of chloroplatinic acid in the flask, adding dropwise the remaining mixture of trimethylsilyl ethene and methyldichlorosilane thereto over a period of 4 hours while stirring the reaction mixture, and continuing the stirring for another 1 hour to complete the reaction. Subsequently, 200 ml of hexane was added to the reaction mixture, and the catalyst precipitated was filtered off. The filtrate was condensed and vaccum-distlled. 145 g (yield: 75%) of (2-trimethylsilylethyl)methyldichlorosilane was obtained.

Workup

  1. customequipped with a dropping funnel
  2. temperaturereflux condenser, stirrer
  3. additionnitrogen gas introducing tube
  4. additionadding dropwise
  5. customstirring for another 1 hour
  6. customthe reaction
  7. customthe catalyst precipitated
  8. filtrationwas filtered off
  9. customcondensed

Sources & evidence

ORD record
ord-d5e57aec5006431697fadef8f86db1ef
Source dataset
uspto-grants-1993_12
Patent number
US05273852

Linked notes

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