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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1178878생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1178878

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 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07276520B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-e338a028fbc14ba2aaed2d5ae3d31166
출처 메모uspto-grants-2007_10