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HRID 276093Erstellt: 25. Oktober 2026

Allylamine → 3-(Dimethoxymethylsilyl)propylamine

https://huagongshe.com/reaction/276093

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllylamineHCID 7853—
Edukt3-(Diethoxymethylsilyl)propylamineHCID 18511—
EduktN-Allyl-1,1,1-trimethyl-N-(trimethylsilyl)silylamineHCID 82125—
EduktMethyldimethoxysilaneHCID 85623—
KatalysatorPlatinumHCID 23939—
LösungsmittelMethanolHCID 887—
Produkt3-(Dimethoxymethylsilyl)propylamineHCID 77233—

Reaktionsschritte

German Patent No. 2408480 describes the reaction of a silazane derivative from allylamine and an organohydrochlorosilane, in the presence of a proton acceptor to form an intermediate silazane which then undergoes a hydrosilylation reaction catalyzed by a platinum catalyst. Upon alcoholysis, the intermediate hydrosilylation product forms 3-aminopropylmethyldiethoxysilane in 70% overall yield. A molar excess of at least 50% of allylamine is used in this process. Identification of the beta-isomer in the product was not made. Japanese Patent No. 10017578 describes another method of synthesis by hydrosilylation of N,N-bis(tri-methylsilyl)allylamine by methyldimethoxysilane. The product of that reaction is then heated with methanol to form 3-aminopropylmethyldimethoxysilane in at least 85% overall yield. The presence of the beta-isomer in the product was not identified. Japanese Patent No. 11209384 describes the use of a rhodium:cyclooctadiene complex as a hydrosilylation catalyst for the addition of methyldiethoxysilane to allylamine to form 3-aminopropylmethyldiethoxy-silane in 78% yield. 2-Aminopropylmethyldiethoxysilane is formed in very low levels in this process not exceeding 0.5%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353073B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-525c10f50d2f4b8ab86217af38d16d3d
Quellennotizuspto-grants-2002_03