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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 504391Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/504391

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, filtered 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
PatentnummerUS07776874B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-b67d6de4eff343b4a4a87926200b9ed2
Quellennotizuspto-grants-2010_08