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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1744691생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1744691

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 (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. (ice cooling). 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 as a colorless liquid (3.50 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07015235B2
출처 데이터셋uspto-grants-2006_03
ORD IDord-f3ebdb4884a54aab8d79f516f6b75fba
출처 메모uspto-grants-2006_03