Methyldiethoxysilane → HCID 23150114, compound

HRID 2099861Notes

Reaction equation

HRID 2099861 reaction equation
[CH2:1]([N:4]1[CH2:9][CH2:8][N:7]([Si:10]([CH3:13])([CH3:12])[CH3:11])[CH2:6][CH2:5]1)[CH:2]=[CH2:3].[CH3:14][SiH:15]([O:19][CH2:20][CH3:21])[O:16][CH2:17][CH3:18]>[Pt].C([Si](C)(C)O[Si](C=C)(C)C)=C.C1(C)C=CC=CC=1>[CH3:14][Si:15]([O:19][CH2:20][CH3:21])([O:16][CH2:17][CH3:18])[CH2:3][CH2:2][CH2:1][N:4]1[CH2:9][CH2:8][N:7]([Si:10]([CH3:11])([CH3:13])[CH3:12])[CH2:6][CH2:5]1

Participants

5

Conditions

Temperature
70 °C

Procedure

A flask equipped with a stirrer, reflux condenser, dropping funnel and thermometer was charged with 99.2 g (0.5 mole) of 1-allyl-4-trimethylsilylpiperazine and 0.65 g of a toluene solution of platinum-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex (platinum content 3 wt %) and heated at 70° C. Once the internal temperature became constant, 67.1 g (0.5 mole) of methyldiethoxysilane was added dropwise over 4 hours. Stirring was continued for a further one hour at the temperature. The reaction solution was distilled, collecting 130.8 g of a fraction having a boiling point of 105-106° C./30 Pa.

Workup

  1. customA flask equipped with a stirrer
  2. temperaturereflux condenser
  3. distillationThe reaction solution was distilled
  4. customcollecting 130.8 g of a fraction

Sources & evidence

ORD record
ord-7b22e133f46343a6a59267fb741a9ed2
Source dataset
uspto-grants-2009_08
Patent number
US07569691B2

Reaction notes

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