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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1178878Erstellt: 26. Oktober 2026

Formaldehyde → N-tert-Butyl-N-(methoxymethyl)-N-(trimethylsilylmethyl)amine

https://huagongshe.com/reaction/1178878

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktMethanolHCID 887—
EduktPotassium CarbonateHCID 11430—
EduktN-tert-Butyl-N-(trimethylsilylmethyl)amineHCID 425246—
LösungsmittelWaterHCID 962—
ProduktN-tert-Butyl-N-(methoxymethyl)-N-(trimethylsilylmethyl)amineHCID 22228418—

Reaktionsschritte

N-tert-Butyl-N-(trimethylsilylmethyl)amine from Step A (8.47 g, 53.1 mmol) was added dropwise, over approximately 30 minutes, via a pressure equalizing addition funnel to a stirred solution of aqueous formaldehyde (5.98 mL of a 37 wt. % solution in water, 79.7 mmol) at 0° C. (ice cooling). After 45 minutes, methanol (6.45 mL, 159.3 mmol) was added and the resulting solution was saturated with potassium carbonate. After stirring vigorously for approximately 5 h, the aqueous phase was removed. The organic phase was saturated with potassium carbonate and stirred overnight. The reaction mixture was poured into water and extracted three times with diethyl ether. The combined organic extracts were washed with brine, dried (MgSO4) and the volatiles evaporated in vacuo. Distillation (high vacuum; ˜70° C.) of the residual liquid afforded the title compound as a colorless liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07276520B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-e338a028fbc14ba2aaed2d5ae3d31166
Quellennotizuspto-grants-2007_10