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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 557928Erstellt: 25. Oktober 2026

Formaldehyde → Benzyl(methoxymethyl)((trimethylsilyl)methyl)amine

https://huagongshe.com/reaction/557928

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktMethanolHCID 887—
EduktPotassium CarbonateHCID 11430—
EduktN-[(Trimethylsilyl)methyl]benzylamineHCID 353458—
LösungsmittelDiethyl EtherHCID 3283—
ProduktBenzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Into a round bottom 3-neck flask equipped with a nitrogen flow and a magnetic stirrer was added formaldehyde (74.000 mmol, 7.4000×10−2 mol) (as a 37% aqueous solution). The flask was cooled to 0° C. and N-benzyl-N-(trimethylsilyl)methylamine (10.000 g, 5.1716790×10−2 mol) was added dropwise with stirring. After stirring for 10 minutes at 0° C., methanol (6.000 mL, 0.14811874 mol) was added in one portion. Potassium carbonate (4.000 g, 2.8942408×10−2 mol) was added to the mixture to absorb the aqueous phase. The mixture was stirred for one hour, then the nonaqueous phase decanted, and then potassium carbonate (2.000 g, 1.4471204×10−2 mol) was added. The mixture was stirred at 25° C. for 12 hours. Ether is added to the mixture and the solution was dried over potassium carbonate, filterd and concentrated under reduced pressure. The residue is distilled at reduced pressure to give the product as a colorless liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08058288B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-683da8e533844a2c94ea096ae7f14482
Quellennotizuspto-grants-2011_11