HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 557928Erstellt: 25. Oktober 2026
Formaldehyde → Benzyl(methoxymethyl)((trimethylsilyl)methyl)amine
https://huagongshe.com/reaction/557928
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Methanol | HCID 887 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | N-[(Trimethylsilyl)methyl]benzylamine | HCID 353458 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Benzyl(methoxymethyl)((trimethylsilyl)methyl)amine | HCID 353442 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08058288B2 |
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| Quelldatensatz | uspto-grants-2011_11 |
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| ORD ID | ord-683da8e533844a2c94ea096ae7f14482 |
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| Quellennotiz | uspto-grants-2011_11 |
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