Methacrylic Acid → Methacryloxymethyltrimethylsilane

HRID 392010

Reaktionsgleichung

Reaktionsgleichung von HRID 392010
[CH3:1][C:2](=[CH2:6])[C:3]([OH:5])=[O:4].Cl[CH2:8][Si:9]([CH3:12])([CH3:11])[CH3:10].C(=O)([O-])[O-].[K+].[K+]>C[N-]C>[CH3:6][C:2](=[CH2:1])[C:3]([O:5][CH2:8][Si:9]([CH3:12])([CH3:11])[CH3:10])=[O:4]

Komponenten

5

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

300 mmol of Methylacrylic acid (MAA) and 200 mmol of chloromethyl trimethylsilane were dissolved in 400 ml of dimethylamide. Potassium carbonate was added to the solution and heated to 90° C. and stirred for 5 hours. Next, the reaction solution was filtered. The filtrate was added to a sodium hydrogen carbonate solution, extracted with ether and pure water respectively, dried, filtered, and concentrated to obtain trimethylsilanylmethyl methylacrylate (TMSA) having the formula (i) below

Aufarbeitung

  1. filtrationNext, the reaction solution was filtered
  2. additionThe filtrate was added to a sodium hydrogen carbonate solution
  3. extractionextracted with ether and pure water respectively
  4. customdried
  5. filtrationfiltered
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-89374aab0d65459ebc755dc684689d3d
Quelldatensatz
uspto-grants-2004_10
Patentnummer
US06800420B2

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