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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29722생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/29722

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물MethanolHCID 887—
반응물Potassium CarbonateHCID 11430—
반응물N-tert-Butyl-N-(trimethylsilylmethyl)amineHCID 425246—
용매WaterHCID 962—
생성물N-tert-Butyl-N-(methoxymethyl)-N-(trimethylsilylmethyl)amineHCID 22228418—

반응 단계

N-tert-Butyl-N-(trimethylsilylmethyl)amine 77 (8.47 g, 53.1 mmol) was added dropwise, over approximately 30 min, 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. After 45 min, 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 78 as a colorless liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419990B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-4be3b5d08bb7443aa7e8a341d9733152
출처 메모uspto-grants-2008_09