Reaktion #1824305

ord-38a12c291fa84b98b0b8e28727ac4691

Reaktionsgleichung

CO[SiH](OC)OC
trimethoxysilane
C=CCOCC1CO1
allyl glycidyl ether
CO[SiH](OC)OC
trimethoxysilane
CO[Si](CCCOCC1CO1)(OC)OC
3-glycidoxypropyltrimethoxysilane
Ausbeute 86.0%

Reaktionsbedingungen

Temperatur
90°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe exotherm of the reaction was controlled with an ice bath
  2. 2
    Temperaturto maintain the temperature at 90°-95° C
  3. 3
    workup.ADDITIONThe addition
  4. 4
    Temperaturtemperature was maintained at 90°-95° C. for another hour

Vorschrift

The apparatus of Example B was charged with 136.8 gm (1.2 mol) of allyl glycidyl ether, 2.6 gm of a carboxylic acid promoter and 0.14 ml of 10% chloroplatinic acid solution. The addition funnel was charged with 122.8 gm (1.0 mol) of trimethoxysilane. The contents of the flask were heated to 90° C. and dropwise addition of trimethoxysilane was begun. The exotherm of the reaction was controlled with an ice bath to maintain the temperature at 90°-95° C. The addition was completed in 25 minutes and temperature was maintained at 90°-95° C. for another hour. Analysis by gas chromatography showed an 86% yield of 3-glycidoxypropyltrimethoxysilane. This example demonstrates a standard preparation of 3-9lycidoxypropyltrimethoxysilane using chloroplatinic acid solution as the catalyst.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE036330uspto-grants-1999_10