Methyldiethoxysilane → HCID 23150114, compound
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]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
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
- customA flask equipped with a stirrer
- temperaturereflux condenser
- distillationThe reaction solution was distilled
- 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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