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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 384570Erstellt: 25. Oktober 2026

Triethylamine → 2-Propenamide, 2-methyl-N-[3-(trimethoxysilyl)propyl]-

https://huagongshe.com/reaction/384570

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethacryloyl chlorideHCID 13528—
EduktAminopropyltrimethoxysilaneHCID 83756—
KatalysatorPhenol, bis(1,1-dimethylethyl)-4-methyl-HCID 3034427—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Propenamide, 2-methyl-N-[3-(trimethoxysilyl)propyl]-HCID 1387916771,6%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

77.4 g 3-(amino)propyltrimethoxysilane, 43.7 g triethylamine and 25 mg di-tert.-butyl-p-cresol were dissolved under argon in 500 ml dichloromethane. 45.1 g methacryloyl chloride was slowly added dropwise at −5° C. within 1 h, and the whole was then stirred for 1 h at 0° C. The precipitated hydrochloride was filtered off and washed with dichloromethane. The volatile constituents were removed at 40° C. under reduced pressure using the rotary evaporator. A yellow liquid with precipitated solid (hydrochloride) remained. The precipitation of the hydrochloride was completed by adding 150 ml diethyl ether, the precipitate was filtered off and the filtrate concentrated at 40° C. using a rotary evaporator with introduction of dry air. The brownish liquid was freed of residual volatile constituents at 4×10−2 mbar, and the raw product (104.2 g) was distilled at a pressure of 6×10−4 mbar. The product had a boiling point of 123-125° C. 76.4 g of product was obtained as yellowish, clear liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367748B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-fba6205435e44ca9aa904b779077e896
Quellennotizuspto-grants-2013_02