(Dimethoxymethylsilyl)benzene → Dicyclohexyldimethoxysilane

HRID 1165980

Reaktionsgleichung

Reaktionsgleichung von HRID 1165980
[CH3:1][Si:2]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)([O:5][CH3:6])[O:3][CH3:4].[H][H]>CCCCCC.[Pd]>[CH:7]1([Si:2]([CH:1]2[CH2:11][CH2:12][CH2:7][CH2:8][CH2:9]2)([O:3][CH3:4])[O:5][CH3:6])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1

Komponenten

5

Versuchsvorschrift

An amount, as set forth in Table 1, of a catalyst constituted by palladium supported on active carbon, sold by DUTRAL Company under the trade name MPT/5, containing 5% by weight of palladium, was loaded, in the form of a suspension in n-hexane at 30% by weight, into an autoclave having a volume of 500 cm3. Then methyl-phenyl-dimethoxy-silane and the solvent were added in the amount, as set forth in the Table, till the volume reached 200 cm3. The mixture was then heated gradually over one hour, under strong stirring, at the temperature and the hydrogen pressure, as set forth in Table 1. After the reaction times indicated hereinbefore, the hydrogenation was practically over. The final mass was cooled, the catalyst was separated by decantation and filtration then the solvent was evaporated. Di-cyclohexyl-dimethoxy-silane was obtained, having a purity of 99.6% and in the amount and with yields as set forth in Table 1.

Aufarbeitung

  1. temperatureThe mixture was then heated gradually over one hour, under strong stirring, at the temperature
  2. customAfter the reaction times
  3. temperatureThe final mass was cooled
  4. customthe catalyst was separated by decantation and filtration
  5. customthe solvent was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-cf87c95741674c528d0439de74f133c3
Quelldatensatz
uspto-grants-1990_03
Patentnummer
US04912243

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