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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1252241Erstellt: 26. Oktober 2026

Triethylamine → 3-Acryloyloxypropyltriphenylsilane

https://huagongshe.com/reaction/1252241

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktAcryloyl chlorideHCID 13140—
Edukt3-(Triphenylsilyl)propan-1-olHCID 4060335—
LösungsmittelBenzeneHCID 241—
Produkt3-AcryloyloxypropyltriphenylsilaneHCID 1414188387,3%

Reaktionsschritte

32.9 g (91.4 mmol) of compound (C) was added to a 1 N solution of sodium carbonate in ethanol and the mixture was heated at 70° to 80° C. for 3 h to conduct the hydrolysis. 27.7 g (87.1 mmol) of 3-hydroxypropyltriphenylsilane (D) was thus obtained (yield: 95.4%). 250 ml of dry benzene was placed in a flask after replacing air in the flask with a dry inert gas (argon). 5.0 g (15.7 mmol) of compound (D) and 1.9 g of triethylamine were dissolved therein. 50 ml of a solution of 1.6 g (17.7 mmol) of acryloyl chloride in benzene was added slowly thereto. After the completion of the addition, the mixture was stirred at room temperature for 6 h. The reaction solution was washed with a 0.5 N hydrochloric acid, water, a 1 N sodium carbonate solution and water successively and then dried over magnesium sulfate. Benzene was distilled off and the residue was purified according to column chromatography (silica gel/benzene) to obtain 5.1 g (13.7 mmol) of 3-acryloyloxypropyltriphenylsilane in the form of white crystals (yield: 87.3%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04742136
Quelldatensatzuspto-grants-1988_05
ORD IDord-947d9dcd3993426a8bd166dc010d2995
Quellennotizuspto-grants-1988_05