돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 557928생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/557928

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물MethanolHCID 887—
반응물Potassium CarbonateHCID 11430—
반응물N-[(Trimethylsilyl)methyl]benzylamineHCID 353458—
용매Diethyl EtherHCID 3283—
생성물Benzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08058288B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-683da8e533844a2c94ea096ae7f14482
출처 메모uspto-grants-2011_11