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HRID 504391作成日:2026年10月26日

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

https://huagongshe.com/reaction/504391

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物MethanolHCID 887—
反応物Potassium CarbonateHCID 11430—
反応物N-[(Trimethylsilyl)methyl]benzylamineHCID 353458—
溶媒Diethyl EtherHCID 3283—
生成物Benzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07776874B2
出典データセットuspto-grants-2010_08
ORD IDord-b67d6de4eff343b4a4a87926200b9ed2
出典メモuspto-grants-2010_08